510(k) K780571
K780571 is an FDA 510(k) premarket notification submitted by C-V Monitors Corp. for the device "BLOOD PRESSURE MODULE". The FDA issued a decision of Substantially Equivalent on May 9, 1978. The device falls under product code DRQ (Amplifier And Signal Conditioner, Transducer Signal), a Class II device regulated under 21 CFR 870.2060. C-V Monitors Corp. has at least 4 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 9, 1978
- Date Received
- April 10, 1978
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Amplifier And Signal Conditioner, Transducer Signal
- Device Class
- Class II
- Regulation Number
- 870.2060
- Review Panel
- CV
- Submission Type