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Toxoplasma Gondii Igg Elisa Kit

by De Ferris Laboratories, Inc. 510(k)

Active United States

510(k) K875258

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK875258 Date30 Sep 1988ClearedStatusActive

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  • Withdrawn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
LGD
Device Class
Class II
Regulation
21 CFR Part 866.3780
Advisory Committee
Microbiology
FDA Decision
SESE Substantially Equivalent

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