FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

CHROMOPHARE D 530 LDR SURGICAL LIGHT

K Number: K990656 · Decision Jul 20, 1999
Classifications
1
FEI Numbers
68
Registration Numbers
68
Same Product Code
73
Applicant Total
16
Review Days
141

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
CHROMOPHARE D 530 LDR SURGICAL LIGHT
K Number
K990656
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4580
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Berchtold Holding GmbH
Date Received
March 1, 1999
Decision Date
July 20, 1999
Product Code
FSY
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FSY Light, Surgical, Ceiling Mounted

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (FSY), ordered by most recent decision date.

View all

Other Clearances by Berchtold Holding GmbH

K Number Device Name
K083066 CHROMOPHARE E 778 AND E 558
K080857 CHROMOPHARE E-SERIES
K024132 CHROMOPHARE X 65
K991527 CHROMOPHARE D500, D530, D650
K974433 CHROMOPHARE D 500, CHROMOPHARE D 530
K965130 CHROMOPHARE
K955750 TELETOM
K950932 BIPOLAP HOOK ELECTRODE
K944855 CHROMOPHARE
K942319 HIRSCH BIPOLAR COAGULATION FORCEPS AND ADAPTOR CABLES
Search all 16 clearances from Berchtold Holding GmbH →