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

RESP-BAC BACTERIA FILTER

K Number: K851070 · Decision Jun 14, 1985
Classifications
1
FEI Numbers
141
Registration Numbers
141
Same Product Code
201
Applicant Total
23
Review Days
88

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Basic Information

Device Name
RESP-BAC BACTERIA FILTER
K Number
K851070
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5260
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Medicomp, Inc.
Date Received
March 18, 1985
Decision Date
June 14, 1985
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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K043454 CARDIOPAL AI WITH DIOGENES SV (CARDIOPAL SV), MODEL PM410
K981119 CARDIOPAL MODEL NUMBER PM20
K952846 EPICARDIA
K943915 HEAT AND MOISTURE EXCHANGER FILTER (HME)
K900207 EPICARDIA 4000
K883103 EPICARDIA PC/FC
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