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Quickscreen Benzodiazepines Screening Test (Numbers 9025 +2 more) - Quickscreen Pro Multi Drug Screening Test Model 1

by Phamatech

510(k) K981687

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK981687 Date3 Jun 1998ClearedStatusActive

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

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  • Withdrawn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
JXM
Models / Variants
Quickscreen Pro Multi Drug Screening Test Model 1
Device Class
Class II
Regulation
21 CFR Part 862.3170
Advisory Committee
Clinical Toxicology
FDA Decision
SESE Substantially Equivalent

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