510(k) K851070

RESP-BAC BACTERIA FILTER by Medicomp, Inc. — Product Code CAH

K851070 is an FDA 510(k) premarket notification submitted by Medicomp, Inc. for the device "RESP-BAC BACTERIA FILTER". The FDA issued a decision of Substantially Equivalent on June 14, 1985. The device falls under product code CAH (Filter, Bacterial, Breathing-Circuit), a Class II device regulated under 21 CFR 868.5260. Medicomp, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 14, 1985
Date Received
March 18, 1985
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Filter, Bacterial, Breathing-Circuit
Device Class
Class II
Regulation Number
868.5260
Review Panel
HO
Submission Type