510(k) K853480

SKYTRON ELITE 6000 & 6001 SURGICAL TABLES by Skytron, Div. the Kmw Group, Inc. — Product Code GDC

K853480 is an FDA 510(k) premarket notification submitted by Skytron, Div. the Kmw Group, Inc. for the device "SKYTRON ELITE 6000 & 6001 SURGICAL TABLES". The FDA issued a decision of Substantially Equivalent on September 12, 1985. The device falls under product code GDC (Table, Operating-Room, Electrical), a Class I device regulated under 21 CFR 878.4960. Skytron, Div. the Kmw Group, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 12, 1985
Date Received
August 20, 1985
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