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

EXAFLEX IMPRESSION MATERIAL (MODIFICATION)

K Number: K955932 · Decision Mar 11, 1996
Classifications
1
FEI Numbers
147
Registration Numbers
147
Same Product Code
399
Applicant Total
98
Review Days
89

Basic Information

Device Name
EXAFLEX IMPRESSION MATERIAL (MODIFICATION)
K Number
K955932
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3660
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
GC AMERICA, INC.
Date Received
December 13, 1995
Decision Date
March 11, 1996
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (ELW), ordered by most recent decision date.

View all

Other Clearances by GC AMERICA, INC.

K Number Device Name
K153231 G-Cem LinkForce, Dual Cure Activator, Try-In Paste, Multi Primer
K153253 GC Reline II
K143140 G-Premio BOND
K141562 MSN-006
K133182 HTFX-222
K133824 CERASMART
K123631 MFP-051
K113816 GC AADVA ABUTMENT- ZIRCONIUM-BO AC BH SV
K120521 GC BLUE SILICONE
K103234 GC AADVA BO AC ABUTMENTS
Search all 98 clearances from GC AMERICA, INC. →