TRI-TECH URINE SPECIMEN KIT— 510(k) K900983

Substantially Equivalent

Tri-Tech, Inc.

FDA 510(k) clearance K900983 for TRI-TECH URINE SPECIMEN KIT, Substantially Equivalent on 1990-09-17. Applicant: Tri-Tech, Inc.. Device class: 1.

Clearance details

Applicant: Tri-Tech, Inc.
Product code: Code FMH
Device class: Class 1
Regulation: 21 CFR 864.3250
Advisory panel: Pathology
Date received: 1990-03-02
Decision date: 1990-09-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Potomac, MD, US

Download summary PDF View on FDA.gov ↗

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