510(k) K761298
K761298 is an FDA 510(k) premarket notification submitted by Mcgaw Respiratory Therapy for the device "PRE-FILLED DISPOSABLE NEBULIZER". The FDA issued a decision of Substantially Equivalent on December 30, 1976. The device falls under product code CAF (Nebulizer (Direct Patient Interface)), a Class II device regulated under 21 CFR 868.5630. Mcgaw Respiratory Therapy has at least 7 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 30, 1976
- Date Received
- December 21, 1976
- 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