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FDA 510(k)

REFERENCE MATERIAL FOR PHENCYCLIDINE IN HUMAN URINE

K-Number: K933557 · 1993-09-10

Decision Date1993-09-10
Product CodeLAS
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

REFERENCE MATERIAL FOR PHENCYCLIDINE IN HUMAN URINE is the device name listed in this FDA 510(k) record. The listed applicant is Consolidated Technologies, Inc.. It received FDA 510(k) clearance on 1993-09-10 under 510(k) number K933557. The device is classified under product code LAS. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REFERENCE MATERIAL FOR PHENCYCLIDINE IN HUMAN URINE?

REFERENCE MATERIAL FOR PHENCYCLIDINE IN HUMAN URINE is a medical device that received FDA 510(k) clearance on 1993-09-10. The listed applicant is Consolidated Technologies, Inc.. The 510(k) number is K933557.

When did REFERENCE MATERIAL FOR PHENCYCLIDINE IN HUMAN URINE receive FDA 510(k) clearance?

REFERENCE MATERIAL FOR PHENCYCLIDINE IN HUMAN URINE received FDA 510(k) clearance on 1993-09-10, under 510(k) number K933557.

Who is the listed applicant for REFERENCE MATERIAL FOR PHENCYCLIDINE IN HUMAN URINE?

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

What is the FDA product code for REFERENCE MATERIAL FOR PHENCYCLIDINE IN HUMAN URINE?

The FDA product code for REFERENCE MATERIAL FOR PHENCYCLIDINE IN HUMAN URINE is LAS.

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 Consolidated Technologies, 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.

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Related Devices (Code: LAS)

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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