FDA.reportPublic FDA data

Vasopress

Primary DI
00815245010062
Brand
Vasopress
Company
COMPRESSION THERAPY CONCEPTS, INC.
Model
VP500DM
Published
2016-09-22
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
JOWSleeve, Limb, Compressible

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
JOWSleeve, Limb, CompressibleCardiovascular2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K101915000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K101915000VASOPRESS SUPREME MINI MODEL VP500DMCompression Therapy Concepts, Inc.2010-08-06JOW

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10815245010076PackageGS16In Commercial Distribution
20815245010080PackageGS1252In Commercial Distribution
00815245010062PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
1081524501007610815245010076
2081524501008020815245010080
00815245010062008152450100628152450100620815245010062

GMDN Terms#

Term, Definition table
TermDefinition
Intermittent venous compression system pumpAn electrically-powered device used for the noninvasive treatment and prevention of venous disorders/sequelae. As part of a compression system, the pump provides the connected stocking/sleeve/suit with the necessary pressure to promote venous blood flow. This is achieved through the cyclical inflation and deflation of a single-chambered stocking/sleeve/suit applied to the extremities. It typically consists of a compressor with control/timing mechanism, pressure limiting device, tubing, and connectors. The resulting increased venous blood flow may help to treat/prevent oedema, deep vein thrombosis (DVT) and pulmonary embolism (PE) in non-ambulatory patients or patients at risk.

Contacts#

Phone, Email table
PhoneEmail
7325440800info@ctcdvt.com

Regulatory Flags#

DUNS number
788065217
Device count
1
Serial number
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00815245010000VasopressVP5002016-09-22
00815245010031VasopressVP500D2016-09-22
00815245010222VasoPressVP5102016-09-22
00815245010253VasoPressVP510L2016-09-22
00815245010284VasoPressVP501P2016-09-22
00815245010338VasoPressVP501M2017-03-09
00815245010383VasoPressVP501L2016-09-22
00815245010437VasoPressVP501B2016-09-22
00815245010536VasoPressVP5202016-09-22
00815245010581VasoPressVP520L2016-09-22
00815245010635VasoPressVP530M2016-09-22
00815245010680VasoPressVP530L2016-09-22
00815245010734VasoPressVP530B2016-09-22
00815245010789VasoPressVP501MG2016-09-22
00815245010833VasoPressVP501LG2016-09-22
00815245010888VasoPressVP530MG2016-09-22
00815245010932VasoPressVP530LG2016-09-22
00815245010987VasoGradVG501M2016-09-22
00815245011038VasoGradVG501L2016-09-22
00815245011083VasoGradVG530M2016-09-22

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
00190446979128AIRCASTDJO, LLCJOW2026-08-03
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50885380194588KendallCardinal Health 200, LLCJOW2026-07-31
50885380194601KendallCardinal Health 200, LLCJOW2026-07-31
50885380194618KendallCardinal Health 200, LLCJOW2026-07-31
50885380194625KendallCardinal Health 200, LLCJOW2026-07-31
50885380194632KendallCardinal Health 200, LLCJOW2026-07-31
50885380194649KendallCardinal Health 200, LLCJOW2026-07-31
50885380194656KendallCardinal Health 200, LLCJOW2026-07-31
50885380194663KendallCardinal Health 200, LLCJOW2026-07-31
50885380194670KendallCardinal Health 200, LLCJOW2026-07-31
50885380194694KendallCardinal Health 200, LLCJOW2026-07-31
10888277348226MEDLINEMEDLINE INDUSTRIES, INC.JOW2026-07-29
10193489024517MEDLINEMEDLINE INDUSTRIES, INC.JOW2026-07-22
10888277348141MEDLINEMEDLINE INDUSTRIES, INC.JOW2026-07-22
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