510(k) K002463

STELLAR by Skytron, Div. the Kmw Group, Inc. — Product Code FSY

K002463 is an FDA 510(k) premarket notification submitted by Skytron, Div. the Kmw Group, Inc. for the device "STELLAR". The FDA issued a decision of Substantially Equivalent on November 8, 2000. The device falls under product code FSY (Light, Surgical, Ceiling Mounted), a Class II device regulated under 21 CFR 878.4580. Skytron, Div. the Kmw Group, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 8, 2000
Date Received
August 10, 2000
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Light, Surgical, Ceiling Mounted
Device Class
Class II
Regulation Number
878.4580
Review Panel
SU
Submission Type