Centria T3 Ria

by Union Carbide Corp. 510(k)

Active United States

510(k) K761305

Regulatory status

as of 28 Oct 2026

Region	Authorization	Number	Date	Status
United States	FDA 510(k)SESE Substantially Equivalent · Traditional	NumberK761305	Date30 Dec 1976Cleared	StatusActive

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not known
Not covered

United States — FDA 510(k) Active

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

510(k)

510(k) Number: K761305
FDA Product Code: CDP

Device Class: Class II
Regulation: 21 CFR Part 862.1710
Advisory Committee: Clinical Chemistry
FDA Decision: SESE Substantially Equivalent

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