510(k) K873475

MICRO-TORQUE HAND ENGINE & ACCESS. DERMABRA. BURS by Mcghan Medical Corp. — Product Code GEY

K873475 is an FDA 510(k) premarket notification submitted by Mcghan Medical Corp. for the device "MICRO-TORQUE HAND ENGINE & ACCESS. DERMABRA. 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