FDA 510(k) FDA class 1 Unknown 🇺🇸 United States

GENERAL SURGERY TRAY

K Number: K940444 · Decision Mar 7, 1994
Classifications
1
FEI Numbers
285
Registration Numbers
286
Same Product Code
21
Applicant Total
23
Review Days
34

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Basic Information

Device Name
GENERAL SURGERY TRAY
K Number
K940444
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Unknown
Statement or Summary
Statement
Applicant
Cush Medical Products
Date Received
February 1, 1994
Decision Date
March 7, 1994
Product Code
LRP
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LRP Tray, Surgical

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Other Clearances by Cush Medical Products

K Number Device Name
K943424 CUSH ISLAND DRESSING
K940518 C-SECTION TRAY
K941349 DENTAL TRAY
K941645 BIOPSY TRAY
K940239 EYE TRAY
K935684 IV START KIT
K941455 STERILE GAUZE PRODUCT LINE
K941522 STERILE X-RAY DETECTABLE GAUZE SPONGES
K941344 LAP SPONGE PRODUCT LINE
K935697 CIRCUMCISION TRAY
Search all 23 clearances from Cush Medical Products →