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FDA 510(k)

NO STEP ON SITE DEUG TEST CUP

K-Number: K012390 · 2001-12-18

ApplicantDrug Free Enterprises
Decision Date2001-12-18
Product CodeLDJ
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

NO STEP ON SITE DEUG TEST CUP is the device name listed in this FDA 510(k) record. The listed applicant is Drug Free Enterprises. It received FDA 510(k) clearance on 2001-12-18 under 510(k) number K012390. The device is classified under product code LDJ. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NO STEP ON SITE DEUG TEST CUP?

NO STEP ON SITE DEUG TEST CUP is a medical device that received FDA 510(k) clearance on 2001-12-18. The listed applicant is Drug Free Enterprises. The 510(k) number is K012390.

When did NO STEP ON SITE DEUG TEST CUP receive FDA 510(k) clearance?

NO STEP ON SITE DEUG TEST CUP received FDA 510(k) clearance on 2001-12-18, under 510(k) number K012390.

Who is the listed applicant for NO STEP ON SITE DEUG TEST CUP?

The FDA 510(k) record lists Drug Free Enterprises as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NO STEP ON SITE DEUG TEST CUP?

The FDA product code for NO STEP ON SITE DEUG TEST CUP is LDJ.

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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.

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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.

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