510(k) K771407
K771407 is an FDA 510(k) premarket notification submitted by Research Development Corp. for the device "LUNG VOLUME & PRESSURE MONITOR". The FDA issued a decision of Substantially Equivalent on August 4, 1977. The device falls under product code BZQ (Monitor, Breathing Frequency), a Class II device regulated under 21 CFR 868.2375. Research Development Corp. has at least 5 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 4, 1977
- Date Received
- July 29, 1977
- 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