FDA.reportPublic FDA data

FaceLake

Primary DI
00851908007024
Brand
FaceLake
Company
LORTE TECHNOLOGIES, INC
Model
CMS-50D Plus
Device description
The CMS-50D Plus finger pulse oximeter is a lightweight, portable device used for measuring both heart rate and blood oxygen levels or SpO2.
Published
2016-10-27
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
OTC
true
Sterile
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
DQAOximeter

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
DQAOximeterCardiovascular2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K082641000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K082641000FINGERTIP PULSE OXIMETER, MODELS CMS-50D, CMS-50L, CMS-50DLContec Medical System Co., Ltd.2008-11-10DQA

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00851908007024PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00851908007024008519080070248519080070240851908007024

GMDN Terms#

Term, Definition table
TermDefinition
Pulse oximeter, battery-poweredA portable, battery-powered, photoelectric device intended for the transcutaneous measurement and display of haemoglobin oxygen saturation (SpO2). The signals, typically produced by light-emitting diodes (LEDs) and a receiving detector in a probe, or directly built-in, are used to make the measurements using the principle of spectrophotometry. The oximeter displays the SpO2 values and may calculate/display other parameters, e.g., pulse rate, electrocardiogram (ECG). The device is typically applied to the fingertip or around the wrist; it may be used by healthcare facilities, emergency services, or in the home.

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
1-847-234-0754info@pulseoximeter.org

Regulatory Flags#

DUNS number
029578633
Device count
1
Serial number
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00851908007055FaceLakeCMS-60D2016-10-27
00851908007000FaceLakeFL-3502016-10-25
00851908007017FaceLakeFL-4002016-10-25
00851908007123FaceLakeFL-4202018-01-17
00851908007222FaceLakeFT822020-12-09
00851908007031FaceLakeCMS-50E2016-10-27
00851908007062FaceLakeCMS-50EW with Bluetooth2016-10-27
00851908007079FaceLakeCMS-50F2016-10-27
00851908007086FaceLakeFL-1002017-03-02
00851908007048FaceLakeSonoline B2016-10-27
00851908007093FaceLakeFL-100B2017-03-02
00851908007109FaceLakeFD-200B2018-01-17
00851908007116FaceLakeFD-200P2018-01-17
00851908007130FaceLakeFD-300P2018-03-21
00851908007161FaceLakeFD-300B2018-03-21

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
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00010939962218N/AShenzhen AOJ Medical Technology Co., LtdDQA2026-07-11
00093351041099N/AShenzhen AOJ Medical Technology Co., LtdDQA2026-07-11
00845717013550N/AShenzhen AOJ Medical Technology Co., LtdDQA2026-07-11
00845717013567N/AShenzhen AOJ Medical Technology Co., LtdDQA2026-07-11
06972040113849N/AShenzhen AOJ Medical Technology Co., LtdDQA2026-07-11
06972040113856N/AShenzhen AOJ Medical Technology Co., LtdDQA2026-07-11
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