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

TELETOM

K Number: K940405 · Decision Apr 14, 1994
Classifications
1
FEI Numbers
102
Registration Numbers
102
Same Product Code
30
Applicant Total
16
Review Days
77

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Basic Information

Device Name
TELETOM
K Number
K940405
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.2400
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Berchtold Holding GmbH
Date Received
January 27, 1994
Decision Date
April 14, 1994
Product Code
KMI
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
KMI Monitor, Bed Patient

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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 →