510(k) K944533

PRIMA, INC. ADULT ANESTHESIA CIRCUIT by Prima, Inc. — Product Code CAI

K944533 is an FDA 510(k) premarket notification submitted by Prima, Inc. for the device "PRIMA, INC. ADULT ANESTHESIA CIRCUIT". The FDA issued a decision of Substantially Equivalent on November 29, 1994. The device falls under product code CAI (Circuit, Breathing (W Connector, Adaptor, Y Piece)), a Class I device regulated under 21 CFR 868.5240. Prima, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 29, 1994
Date Received
September 15, 1994
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Circuit, Breathing (W Connector, Adaptor, Y Piece)
Device Class
Class I
Regulation Number
868.5240
Review Panel
AN
Submission Type