510(k) K760988
K760988 is an FDA 510(k) premarket notification submitted by Adp Intl., Inc. for the device "DENTAL HANDPIECES". The FDA issued a decision of Substantially Equivalent on November 15, 1976. Adp Intl., Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 15, 1976
- Date Received
- October 21, 1976
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No