FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

MIXOMAT AMALGAMATOR

K Number: K914341 · Decision Nov 13, 1991
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
14
Applicant Total
33
Review Days
47

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Basic Information

Device Name
MIXOMAT AMALGAMATOR
K Number
K914341
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.3100
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Degussa AG
Date Received
September 27, 1991
Decision Date
November 13, 1991
Product Code
EFD
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
EFD Amalgamator, Dental, Ac-Powered

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Other Clearances by Degussa AG

K Number Device Name
K953344 DEGUBOND ULTRA
K931808 DUCERAGOLD, DUCERATIN
K926347 DUCERANIUM U
K922790 DEGUCAST 40
K921772 BIOLOR
K921479 DUCERATIN/DUCERAM LFC DENTAL PORCELAIN
K921419 DEVA PLUS
K921445 DEGUBOND PLUS
K914340 DUOMAT 3 AMALGAMATOR
K914368 PART 872 DEGUFILL H & DEGUFILL M DA
Search all 33 clearances from Degussa AG →