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

ROCATEC(R) -PLUS

K Number: K913857 · Decision Dec 16, 1991
Classifications
1
FEI Numbers
94
Registration Numbers
94
Same Product Code
152
Applicant Total
59
Review Days
111

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Basic Information

Device Name
ROCATEC(R) -PLUS
K Number
K913857
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3710
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Espe GmbH (Us)
Date Received
August 27, 1991
Decision Date
December 16, 1991
Product Code
EJH
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

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

Product Code Device Name
EJH Alloy, Metal, Base

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Other Clearances by Espe GmbH (Us)

K Number Device Name
K925027 PHOTAC-FIL APLICAP
K915005 PHOTAC-BOND APLICAP, MODIFICATION
K913966 SONO(R) -CEM
K913965 ESPE(R) -SIL
K905604 VISIO-GEM ART-SYSTEM
K904096 PHOTAC-BOND
K904097 PHOTAC-BOND APLICAP
K904289 PERTAC UNIVERSAL BOND
K900510 PERTAC-HYBRID
K900558 PERTAC BOND
Search all 59 clearances from Espe GmbH (Us) →