510(k) K873476
K873476 is an FDA 510(k) premarket notification submitted by Mcghan Medical Corp. for the device "MINI-MOTOR HAND ENGINE & ACCESS. DERMABRASION BURS". The FDA issued a decision of Substantially Equivalent on September 11, 1987. The device falls under product code GEY (Motor, Surgical Instrument, Ac-Powered), a Class I device regulated under 21 CFR 878.4820. Mcghan Medical Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 11, 1987
- Date Received
- August 31, 1987
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Motor, Surgical Instrument, Ac-Powered
- Device Class
- Class I
- Regulation Number
- 878.4820
- Review Panel
- SU
- Submission Type