510(k) K952014
K952014 is an FDA 510(k) premarket notification submitted by Prima, Inc. for the device "PRIMA ADULT TEMPERATURE MONITORING ANESTHESIA CIRCUITS". The FDA issued a decision of Substantially Equivalent on May 22, 1995. 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
- May 22, 1995
- Date Received
- April 28, 1995
- 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