510(k) K950770

CPR MICROSHIELD II by Plasco, Inc. — Product Code CBP

K950770 is an FDA 510(k) premarket notification submitted by Plasco, Inc. for the device "CPR MICROSHIELD II". The FDA issued a decision of Substantially Equivalent on March 10, 1995. The device falls under product code CBP (Valve, Non-Rebreathing), a Class II device regulated under 21 CFR 868.5870. Plasco, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 10, 1995
Date Received
February 21, 1995
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Valve, Non-Rebreathing
Device Class
Class II
Regulation Number
868.5870
Review Panel
AN
Submission Type