510(k) K864605

VAPLOK by Bear Medical Systems, Inc. — Product Code CAD

K864605 is an FDA 510(k) premarket notification submitted by Bear Medical Systems, Inc. for the device "VAPLOK". The FDA issued a decision of Substantially Equivalent on February 3, 1987. The device falls under product code CAD (Vaporizer, Anesthesia, Non-Heated), a Class II device regulated under 21 CFR 868.5880. Bear Medical Systems, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 3, 1987
Date Received
November 24, 1986
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Vaporizer, Anesthesia, Non-Heated
Device Class
Class II
Regulation Number
868.5880
Review Panel
AN
Submission Type