510(k) K781224
K781224 is an FDA 510(k) premarket notification submitted by Projects IN Health for the device "METER, FLOW, PEAK". The FDA issued a decision of Substantially Equivalent on October 15, 1978. The device falls under product code BZH (Meter, Peak Flow, Spirometry), a Class II device regulated under 21 CFR 868.1860. Projects IN Health has at least 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 15, 1978
- Date Received
- July 17, 1978
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Meter, Peak Flow, Spirometry
- Device Class
- Class II
- Regulation Number
- 868.1860
- Review Panel
- AN
- Submission Type