510(k) K932522

Device
AMSCO STERILE RECOVERIES SURGICAL PACKS
Applicant
AMSCO STERILE RECOVERIES, INC.
510(k) number
K932522
Product code
LRD  
Decision
Substantially Equivalent (SESE)
Decision date
1994-09-09
Date received
1993-05-25
Regulation
874.5220
Classification name
Applicator, Ent Drug
Medical specialty
Ear Nose & Throat
Review panel
Ear Nose & Throat
Device class
1
Clearance type
Traditional
Statement or summary
Statement
Third party reviewed
No

Applicant Contact#

Contact
DENISE A SCHOTTLER
Address
28100 U.S. Hwy., 19n., Suite 201 Clearwater FL US 34621 34621

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code LRD  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K984345AROMAPATCHEnvis, Inc.1999-03-19
K942789MISTASSISTThe Merlin Corp.1994-08-12
K940133THE EXPANDACELL EAR PACKDenver Splint Co.1994-05-23
K925022SURGICAL TRAY (STERILE)Customed, Inc.1993-04-26
K920842AEROSOL DELIVERY SYSTEMSHospitak, Inc.1992-05-15

Legacy Summary#

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FDA Review#

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