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

REGIONAL ANESTHESIA TRAYS

K Number: K965017 · Decision Mar 14, 1997
Classifications
1
FEI Numbers
81
Registration Numbers
81
Same Product Code
154
Applicant Total
22
Review Days
88

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Basic Information

Device Name
REGIONAL ANESTHESIA TRAYS
K Number
K965017
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5140
Medical Specialty
Anesthesiology
Decision
Unknown
Statement or Summary
Summary
Applicant
Smiths Industries Medical Systems, Inc.
Date Received
December 16, 1996
Decision Date
March 14, 1997
Product Code
CAZ
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
CAZ Anesthesia Conduction Kit

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Other Clearances by Smiths Industries Medical Systems, Inc.

K Number Device Name
K972385 FENESTRATED FLEXIBLE D.I.C. TRACHEOSTOMY TUBE CUFFED
K962175 PORTEX ADJUSTABLE FLANGE TRACHEOSTOMY TUBE
K962931 SIMS PRO-VENT 250 (500) PLUS ARTERIAL BLOOD SAMPLING KIT
K963570 SIMS ADULT LUMBAR PUNCTURE KIT (4800-20,4801-20,4806-22,4807-22)
K960429 PER-FIT PERCUTANEOUS TRACHEOSTOMY KIT W/PORTEX TRACHEOSTMY TUBE & DISP. INNER CANNULA
K953485 SIMS CPAP SYSTEM
K953483 SIMS BLUE LINE ENDOBRONCHIAL TUBE
K932946 WALLACE IV CANNULA
K932947 WALLACE Y-CAN
K952516 PRO-VENT, LINE DRAW, PULSATOR
Search all 22 clearances from Smiths Industries Medical Systems, Inc. →