510(k) K932488
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