TRIAGE TOX DRUG SCREEN, MODEL 94400— 510(k) K060791

Substantially Equivalent

Biosite Incorporated

FDA 510(k) clearance K060791 for TRIAGE TOX DRUG SCREEN, MODEL 94400, Substantially Equivalent on 2006-06-22. Applicant: Biosite Incorporated. Device class: 2.

Clearance details

Applicant
Biosite Incorporated
Product code
Code DJR
Device class
Class 2
Regulation
21 CFR 862.3620
Advisory panel
Clinical Toxicology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
San Diego, CA, US
Download summary PDFView on FDA.gov ↗

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Recalls naming K060791

K-number listed on FDA's recall record

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K060791.

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