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FDA 510(k)

ON-SITE ALCOHOL

K-Number: K903223 · 1991-03-13

ApplicantToxi-Lab, Inc.
Decision Date1991-03-13
Product CodeDOJ
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

ON-SITE ALCOHOL is the device name listed in this FDA 510(k) record. The listed applicant is Toxi-Lab, Inc.. It received FDA 510(k) clearance on 1991-03-13 under 510(k) number K903223. The device is classified under product code DOJ. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ON-SITE ALCOHOL?

ON-SITE ALCOHOL is a medical device that received FDA 510(k) clearance on 1991-03-13. The listed applicant is Toxi-Lab, Inc.. The 510(k) number is K903223.

When did ON-SITE ALCOHOL receive FDA 510(k) clearance?

ON-SITE ALCOHOL received FDA 510(k) clearance on 1991-03-13, under 510(k) number K903223.

Who is the listed applicant for ON-SITE ALCOHOL?

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

What is the FDA product code for ON-SITE ALCOHOL?

The FDA product code for ON-SITE ALCOHOL is DOJ.

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Other records listing Toxi-Lab, 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.

K932209TOXI*LAB LTD OPIATE SYSTEMK923337ON*SITE ALCOHOLK901694SPEC(TM) EXTRACTION CARTRIDGEK900626ALPHA URINE SAMPLE

Related Devices (Code: DOJ)

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.

K792469INTERSCI TEST FOR ALCOHOL IN BODY FLUIDSIntersci Corp.

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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