FDA 510(k)

IBD-QUIK CHEK

K-Number: K030704 · 2003-04-21

Decision Date2003-04-21

Product CodeDEG

Advisory CommitteeIM

DecisionSubstantially Equivalent

Device Summary

IBD-QUIK CHEK is the device name listed in this FDA 510(k) record. The listed applicant is Techlab, Inc.. It received FDA 510(k) clearance on 2003-04-21 under 510(k) number K030704. The device is classified under product code DEG. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IBD-QUIK CHEK?

IBD-QUIK CHEK is a medical device that received FDA 510(k) clearance on 2003-04-21. The listed applicant is Techlab, Inc.. The 510(k) number is K030704.

When did IBD-QUIK CHEK receive FDA 510(k) clearance?

IBD-QUIK CHEK received FDA 510(k) clearance on 2003-04-21, under 510(k) number K030704.

Who is the listed applicant for IBD-QUIK CHEK?

The FDA 510(k) record lists Techlab, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IBD-QUIK CHEK?

The FDA product code for IBD-QUIK CHEK is DEG.

Other records listing Techlab, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K191442Campylobacter Chek K191456Campylobacter Quik Chek K181400H. PYLORI CHEK™K181379H. PYLORI QUIK CHEK K173217CAMPYLOBACTER QUIK CHEK K173219CAMPYLOBACTER CHEK

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Related Devices (Code: DEG)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.