FDA 510(k) FDA class 2 Unknown 🇺🇸 United States

DELUXE WOUND CLOSURE TRAY, STERILE, DISPOSABLE

K Number: K921204 · Decision Aug 13, 1992
Classifications
1
FEI Numbers
200
Registration Numbers
200
Same Product Code
449
Applicant Total
44
Review Days
154

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Basic Information

Device Name
DELUXE WOUND CLOSURE TRAY, STERILE, DISPOSABLE
K Number
K921204
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4370
Medical Specialty
General, Plastic Surgery
Decision
Unknown
Statement or Summary
Statement
Applicant
Trinity Laboratories, Inc.
Date Received
March 12, 1992
Decision Date
August 13, 1992
Product Code
KKX
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
KKX Drape, Surgical, Antimicrobial

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K Number Device Name
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K974286 CIRCUMCISION TRAY, CAT. NO. 70340
K972160 CRP-LEX SYSTEM: C-REACTIVE PROTEIN ANTIGEN DETECTION IN SERUM: SLIDE AGGLUTNATION LATEX TEST
K970722 EYE TRAY
K965201 O.R. SCRUB PREP TRAY, STERILE, DISPOSABLE
K964921 BASIC BIOPSY TRAY. DISPOSABLE, STERILE
K953929 MID-STREAM COLLECTION SET-STERILE
K952058 STERILE V.A.D. (VASCULAR ACCESS DEVICES) ACCESS KIT, DISPOSABLE
K953070 WOUNDFOAM 4 X 4
Search all 44 clearances from Trinity Laboratories, Inc. →