AMSCO STERILE RECOVERIES SURGICAL PACKS

Applicator, Ent Drug

AMSCO STERILE RECOVERIES, INC.

The following data is part of a premarket notification filed by Amsco Sterile Recoveries, Inc. with the FDA for Amsco Sterile Recoveries Surgical Packs.

Pre-market Notification Details

Device IDK932522
510k NumberK932522
Device Name:AMSCO STERILE RECOVERIES SURGICAL PACKS
ClassificationApplicator, Ent Drug
Applicant AMSCO STERILE RECOVERIES, INC. 28100 U.S. HWY, 19N., STE. 201 Clearwater,  FL  34621
ContactDenise A Schottler
CorrespondentDenise A Schottler
AMSCO STERILE RECOVERIES, INC. 28100 U.S. HWY, 19N., STE. 201 Clearwater,  FL  34621
Product CodeLRD  
CFR Regulation Number874.5220 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1993-05-25
Decision Date1994-09-09

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