510(k) K880683

KING SYSTEMS, DISP. ANESTHESIA BREATHING CIRCUIT by King Systems Corp. — Product Code CAI

K880683 is an FDA 510(k) premarket notification submitted by King Systems Corp. for the device "KING SYSTEMS, DISP. ANESTHESIA BREATHING CIRCUIT". The FDA issued a decision of Substantially Equivalent on March 9, 1988. The device falls under product code CAI (Circuit, Breathing (W Connector, Adaptor, Y Piece)), a Class I device regulated under 21 CFR 868.5240. King Systems Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 9, 1988
Date Received
February 19, 1988
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