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

CENTRAL VENOUS CATHETER, DRESSING CHANGE KIT, STER

K Number: K920846 · Decision Sep 1, 1992
Classifications
1
FEI Numbers
315
Registration Numbers
315
Same Product Code
606
Applicant Total
44
Review Days
189

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Basic Information

Device Name
CENTRAL VENOUS CATHETER, DRESSING CHANGE KIT, STER
K Number
K920846
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4040
Medical Specialty
General, Plastic Surgery
Decision
Unknown
Statement or Summary
Statement
Applicant
Trinity Laboratories, Inc.
Date Received
February 25, 1992
Decision Date
September 1, 1992
Product Code
FXX
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
FXX Mask, Surgical

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Other Clearances by Trinity Laboratories, Inc.

K Number Device Name
K981441 HEART CATH TRAY, STERILE, DISPOSABLE
K974238 DENTAL TRAY, STERILE, DISPOSABLE
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. →