510(k) K901656
K901656 is an FDA 510(k) premarket notification submitted by Aequitron Medical, Inc. for the device "MODEL 9200 RESPIRATION/HEART RATE MONITOR". The FDA issued a decision of Substantially Equivalent on July 13, 1990. The device falls under product code BZQ (Monitor, Breathing Frequency), a Class II device regulated under 21 CFR 868.2375. Aequitron Medical, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 13, 1990
- Date Received
- April 10, 1990
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Monitor, Breathing Frequency
- Device Class
- Class II
- Regulation Number
- 868.2375
- Review Panel
- AN
- Submission Type