510(k) K955721
K955721 is an FDA 510(k) premarket notification submitted by Mallinckrodt Medical for the device "CUFFED OROPHARYNGEAL AIRWAY (COPA)". The FDA issued a decision of Substantially Equivalent on March 28, 1997. The device falls under product code CAE (Airway, Oropharyngeal, Anesthesiology), a Class I device regulated under 21 CFR 868.5110. Mallinckrodt Medical has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 28, 1997
- Date Received
- December 18, 1995
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Airway, Oropharyngeal, Anesthesiology
- Device Class
- Class I
- Regulation Number
- 868.5110
- Review Panel
- AN
- Submission Type