REDI-TEST COCAINE— 510(k) K991110

Substantially Equivalent

Redwood Biotech, Inc.

FDA 510(k) clearance K991110 for REDI-TEST COCAINE, Substantially Equivalent on 1999-07-26. Applicant: Redwood Biotech, Inc.. Device class: 2.

Clearance details

Applicant: Redwood Biotech, Inc.
Product code: Code DIO
Device class: Class 2
Regulation: 21 CFR 862.3250
Advisory panel: Clinical Toxicology
Date received: 1999-04-01
Decision date: 1999-07-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sunnyvale, CA, US

Download summary PDF View on FDA.gov ↗

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More clearances from Redwood Biotech, Inc.

K000979 — REDI-SCREEN2000-04-10
K993100 — REDI-SCREEN1999-10-06
K991698 — REDI-TEST PCP1999-08-25
K991504 — REDI-TEST METHAMPHETAMINE1999-07-22
K990870 — REDI-TEST THC1999-04-27

Data sourced from openFDA. This site is unofficial and independent of the FDA.