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

WET DRESSING KIT

K Number: K833075 · Decision Jan 27, 1984
Classifications
1
FEI Numbers
329
Registration Numbers
330
Same Product Code
61
Applicant Total
16
Review Days
140

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Basic Information

Device Name
WET DRESSING KIT
K Number
K833075
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Clinipad Corp.
Date Received
September 9, 1983
Decision Date
January 27, 1984
Product Code
KDD
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
KDD Kit, Surgical Instrument, Disposable

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Other Clearances by Clinipad Corp.

K Number Device Name
K931560 CARDIAC CATHETERIZATION TRAY
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K932071 I.V. START KIT
K932010 V.A.D. ACCESS KIT
K932036 LACERATION TRAY
K932016 TRACHEOSTOMY CARE TRAY
K862562 PUNCH BIOPSY KIT
K862563 TRACHEOSTOMY CLEANSING SOLUTION
K833432 CATHETER INSERTION KIT
K830476 OR PREP KIT
Search all 16 clearances from Clinipad Corp. →