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

ZEFON ADULT ANESTHESIA BREATHING CIRCUIT WITH FILTER, ZEFON PEDIATRIC ANESTHESIA BREATHING CIRCUIT WITH FILTER

K Number: K973238 · Decision Mar 11, 1998
Classifications
1
FEI Numbers
141
Registration Numbers
141
Same Product Code
201
Applicant Total
4
Review Days
195

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Basic Information

Device Name
ZEFON ADULT ANESTHESIA BREATHING CIRCUIT WITH FILTER, ZEFON PEDIATRIC ANESTHESIA BREATHING CIRCUIT WITH FILTER
K Number
K973238
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5260
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Bill Olson Corp.
Date Received
August 28, 1997
Decision Date
March 11, 1998
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

Similar 510(k) Clearances

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

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Other Clearances by Bill Olson Corp.

K Number Device Name
K935168 ZEFON PEDIATRIC ANESTHESIA BREATHING CIRCUIT KITS
K911880 ZEFON ADULT ANESTHESIA BREATHING CIRCUIT
K911651 ZEFON BATERIAL/VIRAL FILTER