510(k) K914195

RONDEX CPR NON REBREATHING VALVE #9030, MODIFIED by Rondex Products, Inc. — Product Code CBP

K914195 is an FDA 510(k) premarket notification submitted by Rondex Products, Inc. for the device "RONDEX CPR NON REBREATHING VALVE #9030, MODIFIED". The FDA issued a decision of Substantially Equivalent on November 8, 1991. The device falls under product code CBP (Valve, Non-Rebreathing), a Class II device regulated under 21 CFR 868.5870. Rondex Products, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 8, 1991
Date Received
September 5, 1991
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