FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

CATHETERIZATION INSERTION PACK UROLOGICAL, STERILE, DISPOSABLE

K Number: K951479 · Decision Jun 15, 1995
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
59
Applicant Total
44
Review Days
77

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Basic Information

Device Name
CATHETERIZATION INSERTION PACK UROLOGICAL, STERILE, DISPOSABLE
K Number
K951479
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5130
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Trinity Laboratories, Inc.
Date Received
March 30, 1995
Decision Date
June 15, 1995
Product Code
FCM
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
FCM Tray, Catheterization, Sterile Urethral, With Or Without Catheter (Kit)

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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. →