510(k) K791334
K791334 is an FDA 510(k) premarket notification submitted by Amdia Medical Products for the device "MULTISCOPE". The FDA issued a decision of Substantially Equivalent on August 10, 1979. The device falls under product code DQD (Stethoscope, Electronic), a Class II device regulated under 21 CFR 870.1875. Amdia Medical Products has at least 5 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 10, 1979
- Date Received
- July 20, 1979
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Stethoscope, Electronic
- Device Class
- Class II
- Regulation Number
- 870.1875
- Review Panel
- CV
- Submission Type