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Phenytoin Fpia Reagent Set

by Sigma Diagnostics, Inc. 510(k)

Active United States

510(k) K870953

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK870953 Date31 Mar 1987ClearedStatusActive

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  • Withdrawn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
DIP
Device Class
Class II
Regulation
21 CFR Part 862.3350
Advisory Committee
Clinical Toxicology
FDA Decision
SESE Substantially Equivalent

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