FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

LAP SPONGE PRODUCT LINE

K Number: K941344 · Decision May 12, 1994
Classifications
1
FEI Numbers
228
Registration Numbers
228
Same Product Code
111
Applicant Total
23
Review Days
56

Basic Information

Device Name
LAP SPONGE PRODUCT LINE
K Number
K941344
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4450
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
CUSH MEDICAL PRODUCTS
Date Received
March 17, 1994
Decision Date
May 12, 1994
Product Code
GDY
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
GDY Gauze/Sponge, Internal, X-Ray Detectable

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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
K935697 CIRCUMCISION TRAY
K936120 LABOR AND DELIVERY TRAY
Search all 23 clearances from CUSH MEDICAL PRODUCTS →