FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

ORTHODONTIC ELASTICS

K Number: K810010 · Decision Jan 28, 1981
Classifications
1
FEI Numbers
118
Registration Numbers
118
Same Product Code
24
Applicant Total
2
Review Days
23

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
ORTHODONTIC ELASTICS
K Number
K810010
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.5410
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Orec Corp.
Date Received
January 5, 1981
Decision Date
January 28, 1981
Product Code
ECI
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
ECI Band, Elastic, Orthodontic

Similar 510(k) Clearances

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

View all

Other Clearances by Orec Corp.

K Number Device Name
K803316 ORTHODONTIC BRACKET