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FDA 510(k)

TECHLAB 1-HOUR TOX-A-TEST

K-Number: K931129 · 1993-09-30

ApplicantTechlab, Inc.
Decision Date1993-09-30
Product CodeLLH
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

TECHLAB 1-HOUR TOX-A-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 1993-09-30 under 510(k) number K931129. 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 TECHLAB 1-HOUR TOX-A-TEST?

TECHLAB 1-HOUR TOX-A-TEST is a medical device that received FDA 510(k) clearance on 1993-09-30. The listed applicant is Techlab, Inc.. The 510(k) number is K931129.

When did TECHLAB 1-HOUR TOX-A-TEST receive FDA 510(k) clearance?

TECHLAB 1-HOUR TOX-A-TEST received FDA 510(k) clearance on 1993-09-30, under 510(k) number K931129.

Who is the listed applicant for TECHLAB 1-HOUR TOX-A-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 TECHLAB 1-HOUR TOX-A-TEST?

The FDA product code for TECHLAB 1-HOUR TOX-A-TEST is LLH.

Related Clinical Trials

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.

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.

View all 36 devices →

Related Devices (Code: LLH)

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.

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.

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