FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

RACEGEL

K Number: K093711 · Decision Feb 17, 2010
Classifications
1
FEI Numbers
40
Registration Numbers
40
Same Product Code
35
Applicant Total
9
Review Days
78

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
RACEGEL
K Number
K093711
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Septodont
Date Received
December 1, 2009
Decision Date
February 17, 2010
Product Code
MVL
Advisory Committee
Unknown
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
MVL Cord, Retraction

Similar 510(k) Clearances

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

View all

Other Clearances by Septodont

K Number Device Name
K212283 BioRoot Flow 0.5g, BioRoot Flow 2g
K211799 Biodentine XP 500, Biodentine XP 200
K172839 ENDOSOLV
K140132 BIODENTINE
K092251 BIODENTINE
K063634 RTR SYRINGE
K051010 SECURALLOY, SEPTALLOY NG 50 AND SEPTALLOY NG 70
K032708 PLASTALGIN AND PLASTALGIN ORTHO