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

GINGITRACT

K Number: K771973 · Decision Nov 7, 1977
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
7
Applicant Total
29
Review Days
21

Basic Information

Device Name
GINGITRACT
K Number
K771973
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.4565
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
DEN-MAT CORP.
Date Received
October 17, 1977
Decision Date
November 7, 1977
Product Code
EIG
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
EIG Retractor, All Types

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K875351 DEN-MAT PORETCH (PORCELAIN ETCHANT)
K872510 DEN-MAT TENURE
K870130 DEN-MAT SECURE ANTI-ROTATIONAL POST-CORE SYSTEM
K864346 REMBRANDT PORCELAIN TINTING KIT
K862449 DEN-MAT DENTIN LINK
K860971 DEN-MAT GOLD LINK (FORMERLY DEN-MAT METAL OPAQUER)
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