510(k) K792112
K792112 is an FDA 510(k) premarket notification submitted by Conphar, Inc. for the device "CONPHAR STETHSCOPE". The FDA issued a decision of Substantially Equivalent on Dec 4, 1979. The device falls under product code DQD (Stethoscope, Electronic), a Class II device regulated under 21 CFR 870.1875. Conphar, Inc. has 121 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Dec 4, 1979
- Date Received
- Oct 25, 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
- 510(k)