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

PRESSURE TUBING AND ACCESSORIES

K Number: K901816 · Decision Jul 12, 1990
Classifications
1
FEI Numbers
141
Registration Numbers
141
Same Product Code
201
Applicant Total
15
Review Days
80

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Basic Information

Device Name
PRESSURE TUBING AND ACCESSORIES
K Number
K901816
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5260
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Arbo Medical, Inc.
Date Received
April 23, 1990
Decision Date
July 12, 1990
Product Code
CAH
Advisory Committee
Anesthesiology
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
CAH Filter, Bacterial, Breathing-Circuit

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Other Clearances by Arbo Medical, Inc.

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K935437 ARBO H85V/H87V/H27V DISPOS MONIT ELECTRODES
K942905 DISPOSABLE TEMPERATURE PROBE COVER
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
Search all 15 clearances from Arbo Medical, Inc. →