FDA 510(k) FDA class 1 Substantially Equivalent 🇩🇪 Germany

CHROMOPHARE

K Number: K935832 · Decision Feb 3, 1994
Classifications
1
FEI Numbers
90
Registration Numbers
90
Same Product Code
36
Applicant Total
16
Review Days
58

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Basic Information

Device Name
CHROMOPHARE
K Number
K935832
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6320
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Berchtold Holding GmbH
Date Received
December 7, 1993
Decision Date
February 3, 1994
Product Code
KZF
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
KZF Device, Medical Examination, Ac Powered

Similar 510(k) Clearances

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

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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
K990656 CHROMOPHARE D 530 LDR SURGICAL LIGHT
K991527 CHROMOPHARE D500, D530, D650
K974433 CHROMOPHARE D 500, CHROMOPHARE D 530
K965130 CHROMOPHARE
K955750 TELETOM
K950932 BIPOLAP HOOK ELECTRODE
K944855 CHROMOPHARE
Search all 16 clearances from Berchtold Holding GmbH →