510(k) K792466
K792466 is an FDA 510(k) premarket notification submitted by Nicolet Biomedical Instruments for the device "NIC-200 VENTRICULAR FUNCTION ANALYZER". The FDA issued a decision of Substantially Equivalent on January 24, 1980. The device falls under product code DQC (Phonocardiograph), a Class I device regulated under 21 CFR 870.2390. Nicolet Biomedical Instruments has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 24, 1980
- Date Received
- December 3, 1979
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Phonocardiograph
- Device Class
- Class I
- Regulation Number
- 870.2390
- Review Panel
- CV
- Submission Type