510(k) K913266

MICRO-AIRE MODEL 2050E/ELEC HANDPIECE/TROTTLELESS by Micro Surgical Instruments Corp. — Product Code GEY

K913266 is an FDA 510(k) premarket notification submitted by Micro Surgical Instruments Corp. for the device "MICRO-AIRE MODEL 2050E/ELEC HANDPIECE/TROTTLELESS". The FDA issued a decision of Substantially Equivalent on October 21, 1991. The device falls under product code GEY (Motor, Surgical Instrument, Ac-Powered), a Class I device regulated under 21 CFR 878.4820. Micro Surgical Instruments Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 21, 1991
Date Received
July 23, 1991
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