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

PRE-CUT TRACHEOSTOMY DRESSING STERILE, DISPOSABLE

K Number: K920282 · Decision May 29, 1992
Classifications
1
FEI Numbers
570
Registration Numbers
570
Same Product Code
87
Applicant Total
44
Review Days
128

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Basic Information

Device Name
PRE-CUT TRACHEOSTOMY DRESSING STERILE, DISPOSABLE
K Number
K920282
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4014
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Trinity Laboratories, Inc.
Date Received
January 22, 1992
Decision Date
May 29, 1992
Product Code
NAB
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
NAB Gauze / Sponge,Nonresorbable For External Use

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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. →