510(k) K883613

OPER. TABLE FOR PERCUTAN. TRANS. CORONARY ANGIO. by Stierlen-Maquet AG — Product Code GDC

K883613 is an FDA 510(k) premarket notification submitted by Stierlen-Maquet AG for the device "OPER. TABLE FOR PERCUTAN. TRANS. CORONARY ANGIO.". The FDA issued a decision of Substantially Equivalent on September 15, 1988. The device falls under product code GDC (Table, Operating-Room, Electrical), a Class I device regulated under 21 CFR 878.4960. Stierlen-Maquet AG has at least 9 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 15, 1988
Date Received
August 22, 1988
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Table, Operating-Room, Electrical
Device Class
Class I
Regulation Number
878.4960
Review Panel
SU
Submission Type