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

EXTRACORPOREAL TEMPERATURE SENSOR

K Number: K935603 · Decision Feb 15, 1994
Classifications
1
FEI Numbers
488
Registration Numbers
488
Same Product Code
797
Applicant Total
22
Review Days
89

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
EXTRACORPOREAL TEMPERATURE SENSOR
K Number
K935603
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.2910
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Smiths Industries Medical Systems, Inc.
Date Received
November 18, 1993
Decision Date
February 15, 1994
Product Code
FLL
Advisory Committee
General Hospital
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
FLL Continuous Measurement Thermometer

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (FLL), ordered by most recent decision date.

View all

Other Clearances by Smiths Industries Medical Systems, Inc.

K Number Device Name
K972385 FENESTRATED FLEXIBLE D.I.C. TRACHEOSTOMY TUBE CUFFED
K965017 REGIONAL ANESTHESIA TRAYS
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
Search all 22 clearances from Smiths Industries Medical Systems, Inc. →