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

SUCTION CATHETER KIT, STERILE, SINGLE-USE

K Number: K951506 · Decision Jul 3, 1995
Classifications
1
FEI Numbers
245
Registration Numbers
245
Same Product Code
115
Applicant Total
44
Review Days
91

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Basic Information

Device Name
SUCTION CATHETER KIT, STERILE, SINGLE-USE
K Number
K951506
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.6810
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Trinity Laboratories, Inc.
Date Received
April 3, 1995
Decision Date
July 3, 1995
Product Code
BSY
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
BSY Catheters, Suction, Tracheobronchial

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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. →