Skip to content

Incstar 25-Hydroxyvitmin D 1251 Ria

by Incstar Corp.

510(k) K953567

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None ongoing

1 closed

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 9 Oct 2026. What this means

Regulatory status

as of registry sync 9 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK953567 Date25 Sep 1996ClearedStatusActive

Recalls

1 recall · FDA

    • Terminated Z-1237-2007 FDA Unclassified (pre-2012) initiated 21 Aug 2007

    25 Hydroxyvitamin D RIA kits may contain the incorrect lot of tracer.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA Product Code
MRG
Device Class
Class II
Regulation
21 CFR Part 862.1825
Advisory Committee
Clinical Chemistry
FDA Decision
SESE Substantially Equivalent

Other devices from Incstar Corp.

See all devices from Incstar Corp. →