510(k) K932488

PMP, LTD. PEDIATRIC GAS SAMPLING CIRCUITS by Precision Med Products, Ltd. — Product Code CAI

K932488 is an FDA 510(k) premarket notification submitted by Precision Med Products, Ltd. for the device "PMP, LTD. PEDIATRIC GAS SAMPLING CIRCUITS". The FDA issued a decision of Substantially Equivalent on July 22, 1993. The device falls under product code CAI (Circuit, Breathing (W Connector, Adaptor, Y Piece)), a Class I device regulated under 21 CFR 868.5240. Precision Med Products, Ltd. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 22, 1993
Date Received
May 24, 1993
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