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

PERMADYNE POLYETHER RUBBER IMPRESSION

K Number: K800031 · Decision Feb 5, 1980
Classifications
1
FEI Numbers
143
Registration Numbers
143
Same Product Code
401
Applicant Total
8
Review Days
29

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Basic Information

Device Name
PERMADYNE POLYETHER RUBBER IMPRESSION
K Number
K800031
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3660
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Espe Dental Products
Date Received
January 7, 1980
Decision Date
February 5, 1980
Product Code
ELW
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
ELW Material, Impression

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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
K771889 UNIOLITE
K771901 CAPMIX
K771120 IMPREFLEX ALGINATE IMPRESSION MATERIAL
K771119 PASTES, RESTORATIVE & TINTED, DEBTAL