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Verdict Barbiturates

by Editek, Inc. 510(k)

Active United States

510(k) K963529

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK963529 Date30 Oct 1996ClearedStatusActive

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  • Withdrawn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 22 Oct 2026.

Specification

510(k)

510(k) Number
FDA Product Code
DIS
Device Class
Class II
Regulation
21 CFR Part 862.3150
Advisory Committee
Clinical Toxicology
FDA Decision
SESE Substantially Equivalent

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