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

CAPMIX

K Number: K771901 · Decision Oct 20, 1977
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
14
Applicant Total
8
Review Days
13

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Basic Information

Device Name
CAPMIX
K Number
K771901
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.3100
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Espe Dental Products
Date Received
October 7, 1977
Decision Date
October 20, 1977
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 Espe Dental Products

K Number Device Name
K810950 VISIO-SEAL
K802819 KETAC-CEM IN REF. TO K802048
K802049 NIMETIC-DISPERS
K800031 PERMADYNE POLYETHER RUBBER IMPRESSION
K771889 UNIOLITE
K771120 IMPREFLEX ALGINATE IMPRESSION MATERIAL
K771119 PASTES, RESTORATIVE & TINTED, DEBTAL