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Diagnon B12 57CO Ria Kit

by Diagnon Corp. 510(k)

Active United States

510(k) K832717

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK832717 Date8 Dec 1983ClearedStatusActive

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Recalls

0 recalls · FDA

No FDA recalls on record, checked 11 Oct 2026.

Specification

510(k)

510(k) Number
FDA Product Code
CDD
Device Class
Class II
Regulation
21 CFR Part 862.1810
Advisory Committee
Clinical Chemistry
FDA Decision
SESE Substantially Equivalent

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