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

CERAMIST BRUSH

K Number: K770160 · Decision Jan 31, 1977
Classifications
1
FEI Numbers
105
Registration Numbers
105
Same Product Code
2
Applicant Total
46
Review Days
7

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Basic Information

Device Name
CERAMIST BRUSH
K Number
K770160
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.3140
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Deringer-Ney, Inc.
Date Received
January 24, 1977
Decision Date
January 31, 1977
Product Code
KXR
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
KXR Applicator, Resin

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Other Clearances by Deringer-Ney, Inc.

K Number Device Name
K933178 GDC 3509
K930482 DENTAL CASTING ALLOY, MODIFICATION - PF-3
K930481 DENTAL CASTING ALLOY MODIFICATION-PF-4
K925273 GDC 3445
K920922 GDC 3367
K920060 DENTAL SOLDER ALLOY
K920887 GDC-3338, DENTAL SOLDER ALLOY
K910065 GDC-3200 DENTAL SOLDER
K904695 GDC-1501
K904614 GDC-1475
Search all 46 clearances from Deringer-Ney, Inc. →