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FDA 510(k)

TOX A/B TEST

K-Number: K971182 · 1997-07-22

ApplicantTechlab, Inc.
Decision Date1997-07-22
Product CodeLLH
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

TOX A/B TEST is the device name listed in this FDA 510(k) record. The listed applicant is Techlab, Inc.. It received FDA 510(k) clearance on 1997-07-22 under 510(k) number K971182. The device is classified under product code LLH. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TOX A/B TEST?

TOX A/B TEST is a medical device that received FDA 510(k) clearance on 1997-07-22. The listed applicant is Techlab, Inc.. The 510(k) number is K971182.

When did TOX A/B TEST receive FDA 510(k) clearance?

TOX A/B TEST received FDA 510(k) clearance on 1997-07-22, under 510(k) number K971182.

Who is the listed applicant for TOX A/B TEST?

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 TOX A/B TEST?

The FDA product code for TOX A/B TEST is LLH.

Other records listing Techlab, Inc. as applicant

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Related Devices (Code: LLH)

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Official Source

View on FDA Database →

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

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