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

BREATHING CIRCUIT BACTERIA FILTER

K Number: K831856 · Decision Sep 26, 1983
Classifications
1
FEI Numbers
141
Registration Numbers
141
Same Product Code
201
Applicant Total
75
Review Days
109

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Basic Information

Device Name
BREATHING CIRCUIT BACTERIA FILTER
K Number
K831856
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5260
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Vital Signs, Inc.
Date Received
June 9, 1983
Decision Date
September 26, 1983
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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K022402 DISPOSABLE PRESSURE MANOMETER
K021315 SURE-LOK
K002454 BREAS HA50 HUMIDIFIER, MODEL HA50
K001553 BREAS PV 100 CPAP SYSTEM
K000441 BODYGUARD
K994044 CLEEN-ABLE
K990412 CUFF-ABLE PLUS
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