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

SUTURE REMOVAL KIT

K Number: K922339 · Decision Dec 11, 1992
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
14
Applicant Total
21
Review Days
206

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Basic Information

Device Name
SUTURE REMOVAL KIT
K Number
K922339
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Unknown
Statement or Summary
Statement
Applicant
Transidyne General Corp.
Date Received
May 19, 1992
Decision Date
December 11, 1992
Product Code
MCZ
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
MCZ Suture Removal Kit

Similar 510(k) Clearances

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Other Clearances by Transidyne General Corp.

K Number Device Name
K961217 BODILY FLUID DISPOSAL KIT
K955658 LACERATION TRAY
K950773 PROPHYLAXIS PACK
K950743 ORAL PROCEDURE PACK
K950449 SURGICAL BUR
K950403 SURGICAL SAW BLADES
K924811 I.V. START KIT
K924243 TRACHEOSTOMY CARE KIT
K922041 PRIMARY SURGICAL DRESSING TRAY
K897133 MODEL 1050 - UMBILICAL CORD BLOOD SAMPLING KIT
Search all 21 clearances from Transidyne General Corp. →