510(k) K991527

CHROMOPHARE D500, D530, D650 by Berchtold Holding GmbH — Product Code FSY

K991527 is an FDA 510(k) premarket notification submitted by Berchtold Holding GmbH for the device "CHROMOPHARE D500, D530, D650". The FDA issued a decision of Substantially Equivalent on May 27, 1999. The device falls under product code FSY (Light, Surgical, Ceiling Mounted), a Class II device regulated under 21 CFR 878.4580. Berchtold Holding GmbH has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 27, 1999
Date Received
May 3, 1999
Clearance Type
Special
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