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

TESCERA GLAZING RESIN, MODEL T-1804, BISCOVER XT, MODEL G-93220P

K Number: K024046 · Decision Feb 6, 2003
Classifications
1
FEI Numbers
43
Registration Numbers
43
Same Product Code
51
Applicant Total
88
Review Days
62

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
TESCERA GLAZING RESIN, MODEL T-1804, BISCOVER XT, MODEL G-93220P
K Number
K024046
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3310
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Bisco, Inc.
Date Received
December 6, 2002
Decision Date
February 6, 2003
Product Code
EBD
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
EBD Coating, Filling Material, Resin

Similar 510(k) Clearances

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

View all

Other Clearances by Bisco, Inc.

K Number Device Name
K250156 Choice 2 DC
K242816 Quantium
K192007 TheraBase, TheraBase Ca
K182917 FluoroCal
K180344 TheraCal DC
K171147 REVEAL Bulk
K162598 HAPI Seal
K163171 CeraClean
K161051 All-Bond Universal w/BAC (not finalized)
K161256 TheraCem
Search all 88 clearances from Bisco, Inc. →