CAMPYLOBACTER QUIK CHEK— 510(k) K173217

Substantially Equivalent

Techlab, Inc.

FDA 510(k) clearance K173217 for CAMPYLOBACTER QUIK CHEK, Substantially Equivalent on 2018-01-22. Applicant: Techlab, Inc.. Device class: 1.

Clearance details

Applicant: Techlab, Inc.
Product code: Code LQP
Device class: Class 1
Regulation: 21 CFR 866.3110
Advisory panel: Microbiology
Date received: 2017-10-03
Decision date: 2018-01-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Blacksburg, VA, US

Download summary PDF View on FDA.gov ↗

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More clearances from Techlab, Inc.

K181379 — H. PYLORI QUIK CHEK2018-08-21
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K171078 — TRI-COMBO PARASITE SCREEN2017-07-10
K170728 — E. HISTOLYTICA QUIK CHEK2017-06-07
K082499 — C. DIFF QUIK CHEK COMPLETE2009-03-26

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