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

MAINFLOW BACTERIA FILTER

K Number: K801803 · Decision Aug 13, 1980
Classifications
1
FEI Numbers
141
Registration Numbers
141
Same Product Code
201
Applicant Total
10
Review Days
15

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Basic Information

Device Name
MAINFLOW BACTERIA FILTER
K Number
K801803
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5260
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Omnicon Medical Corp.
Date Received
July 29, 1980
Decision Date
August 13, 1980
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 Omnicon Medical Corp.

K Number Device Name
K823872 EMERGENCY TRACHEOSTOMY KIT
K820577 ANESTHESIA BACTERIA FILTER
K820576 MAINFLOW BACTERIA FILTER
K801804 ANESTHESIA BACTERIA FILTER
K772060 PROTECT IV GARD
K770136 DISPOSABLE BACTERIA FILTER
K770001 AIRWAY, BERMAN 40, 60, 80, 90, L00MM'S
K760819 CONDUCTIVE ANESTHESIA BREATHING CIRCUIT
K760149 CONDUCTIVE ANESTHSIA BREATH. CIRCUIT