510(k) K914465
K914465 is an FDA 510(k) premarket notification submitted by Pegasus Research Corp. for the device "AUTOCLAVABLE VERSION THERA-MIST NEBULIZER, P32000". The FDA issued a decision of Substantially Equivalent on March 31, 1992. The device falls under product code CAF (Nebulizer (Direct Patient Interface)), a Class II device regulated under 21 CFR 868.5630. Pegasus Research Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 31, 1992
- Date Received
- October 7, 1991
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Nebulizer (Direct Patient Interface)
- Device Class
- Class II
- Regulation Number
- 868.5630
- Review Panel
- AN
- Submission Type