LACERATION TRAY

Wound Dressing Kit

MEDICAL DEVICE INSPECTION CO., INC.

The following data is part of a premarket notification filed by Medical Device Inspection Co., Inc. with the FDA for Laceration Tray.

Pre-market Notification Details

Device IDK912117
510k NumberK912117
Device Name:LACERATION TRAY
ClassificationWound Dressing Kit
Applicant MEDICAL DEVICE INSPECTION CO., INC. 55 NORTHERN BLVD. SUITE 301 Great Neck,  NY  11021
ContactAlan P Schwartz
CorrespondentAlan P Schwartz
MEDICAL DEVICE INSPECTION CO., INC. 55 NORTHERN BLVD. SUITE 301 Great Neck,  NY  11021
Product CodeMCY  
CFR Regulation Number880.5075 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1991-05-13
Decision Date1991-08-09

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