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

FLUOREVER(R) DUAL CURE CERAMIC VENEER CEMENT

K Number: K890623 · Decision Apr 17, 1989
Classifications
1
FEI Numbers
144
Registration Numbers
144
Same Product Code
504
Applicant Total
5
Review Days
69

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
FLUOREVER(R) DUAL CURE CERAMIC VENEER CEMENT
K Number
K890623
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3275
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Macrochem Corp.
Date Received
February 7, 1989
Decision Date
April 17, 1989
Product Code
EMA
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
EMA Cement, Dental

Similar 510(k) Clearances

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

View all

Other Clearances by Macrochem Corp.

K Number Device Name
K890608 FLUOREVER(R) LIGHT CURE CERAMIC VENEER CEMENT
K890494 FLUOREVER PIT AND FISSURE SEALANT OR FLUOREVER PFS
K880562 ADDITIONAL CLAIMS TO DENTAL RESTORATIVE COMP. KIT
K861546 REPLICA-F VISIBLE LIGHT-CURED ANT/POST DEN COM KIT