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

DISPOSABLE TEMPERATURE PROBE COVER

K Number: K942905 · Decision Feb 27, 1995
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
91
Applicant Total
15
Review Days
251

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Basic Information

Device Name
DISPOSABLE TEMPERATURE PROBE COVER
K Number
K942905
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5130
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Arbo Medical, Inc.
Date Received
June 21, 1994
Decision Date
February 27, 1995
Product Code
FMT
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
FMT Warmer, Infant Radiant

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Other Clearances by Arbo Medical, Inc.

K Number Device Name
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K935437 ARBO H85V/H87V/H27V DISPOS MONIT ELECTRODES
K940302 ARBO MONITRING SAFETY CABLE & LEAD WIRE SYSTEMS/ARBO UNSHEILDED SAFETY CABLE & LEAD SYSTEM
K940322 ARBO VS MONITOR CABLE & LEADWIRE SYSTEM ARBO SHIELDED SAFETY CABLE & LEAD WIRE
K935246 ARBO H49P, H59P DISPOSABLE MONITORING ELECTRODES
K935429 ARBO H90, H91, H135 DISPOSABLE MONITORING ELECTRODES
K935281 ARBO H87P, H85P, H27P DISPOSABLE MONITORING ELECTRODES
K905545 ULTRASOUND TRANSMISSION GEL
K902788 CLEM TM
K901816 PRESSURE TUBING AND ACCESSORIES
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