510(k) K873359

AIRLIFE VOLUME VENTI. CIRCUIT W/CLEAR CAP EX VALVE by American Pharmaseal Div. Ahsc — Product Code CAI

K873359 is an FDA 510(k) premarket notification submitted by American Pharmaseal Div. Ahsc for the device "AIRLIFE VOLUME VENTI. CIRCUIT W/CLEAR CAP EX VALVE". The FDA issued a decision of Substantially Equivalent on November 6, 1987. The device falls under product code CAI (Circuit, Breathing (W Connector, Adaptor, Y Piece)), a Class I device regulated under 21 CFR 868.5240. American Pharmaseal Div. Ahsc has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 6, 1987
Date Received
August 21, 1987
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