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

KWIKAP

K Number: K772315 · Decision Jan 3, 1978
Classifications
1
FEI Numbers
71
Registration Numbers
71
Same Product Code
10
Applicant Total
29
Review Days
15

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Basic Information

Device Name
KWIKAP
K Number
K772315
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.3275
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Den-Mat Corp.
Date Received
December 19, 1977
Decision Date
January 3, 1978
Product Code
EMB
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
EMB Zinc Oxide Eugenol

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Other Clearances by Den-Mat Corp.

K Number Device Name
K983106 1ST IMPRESSION
K895731 DEN-MAT CERINATE PORCELAIN
K895269 DEN-MAT LAMI-QUICK
K881918 LIGHT-CURED ZIONOMER CEMENT
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)
Search all 29 clearances from Den-Mat Corp. →