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

SUTURE REMOVAL KIT

K Number: K803199 · Decision Jan 15, 1981
Classifications
1
FEI Numbers
329
Registration Numbers
330
Same Product Code
61
Applicant Total
11
Review Days
29

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Basic Information

Device Name
SUTURE REMOVAL KIT
K Number
K803199
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Walpak Co.
Date Received
December 17, 1980
Decision Date
January 15, 1981
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 Walpak Co.

K Number Device Name
K803200 IRRIGATION SET W/BULB SYRINGE
K803204 IRRIGATION PISTON
K803198 IRRIGATION SET W/PISTON SYRINGE
K803201 LEMON GLYCERINE SWABS
K802083 CATHETER INSERTION TRAY
K791598 CLOSED SYSTEM FOLEY CATHERIZATION PROCED
K780123 CATHETERIZATION PROCEDURE TRAY
K780124 CATHETERIZATION PROCED. TRAY, URETHRAL
K770446 SPONGES, LAPAROTOMY
K760560 CATH CARE KIT
Search all 11 clearances from Walpak Co. →