FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

BIOLOR

K Number: K921772 · Decision Jul 13, 1992
Classifications
1
FEI Numbers
42
Registration Numbers
42
Same Product Code
626
Applicant Total
33
Review Days
90

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Basic Information

Device Name
BIOLOR
K Number
K921772
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3060
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Degussa AG
Date Received
April 14, 1992
Decision Date
July 13, 1992
Product Code
EJT
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
EJT Alloy, Gold-Based Noble Metal

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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
K921479 DUCERATIN/DUCERAM LFC DENTAL PORCELAIN
K921419 DEVA PLUS
K921445 DEGUBOND PLUS
K914340 DUOMAT 3 AMALGAMATOR
K914341 MIXOMAT AMALGAMATOR
K914368 PART 872 DEGUFILL H & DEGUFILL M DA
Search all 33 clearances from Degussa AG →