510(k) K832188

HALL RECIPROCATOR by Amsco Co. — Product Code GET

K832188 is an FDA 510(k) premarket notification submitted by Amsco Co. for the device "HALL RECIPROCATOR". The FDA issued a decision of Substantially Equivalent on August 12, 1983. The device falls under product code GET (Motor, Surgical Instrument, Pneumatic Powered), a Class I device regulated under 21 CFR 878.4820. Amsco Co. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 12, 1983
Date Received
July 6, 1983
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Motor, Surgical Instrument, Pneumatic Powered
Device Class
Class I
Regulation Number
878.4820
Review Panel
SU
Submission Type