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FDA 510(k)

PHENCYCLIDINE EIA ASSAY, MODIFICATION

K-Number: K920957 · 1992-03-18

ApplicantDiagnostic Reagents, Inc.
Decision Date1992-03-18
Product CodeLCM
DecisionSubstantially Equivalent

Device Summary

PHENCYCLIDINE EIA ASSAY, MODIFICATION is the device name listed in this FDA 510(k) record. The listed applicant is Diagnostic Reagents, Inc.. It received FDA 510(k) clearance on 1992-03-18 under 510(k) number K920957. The device is classified under product code LCM. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHENCYCLIDINE EIA ASSAY, MODIFICATION?

PHENCYCLIDINE EIA ASSAY, MODIFICATION is a medical device that received FDA 510(k) clearance on 1992-03-18. The listed applicant is Diagnostic Reagents, Inc.. The 510(k) number is K920957.

When did PHENCYCLIDINE EIA ASSAY, MODIFICATION receive FDA 510(k) clearance?

PHENCYCLIDINE EIA ASSAY, MODIFICATION received FDA 510(k) clearance on 1992-03-18, under 510(k) number K920957.

Who is the listed applicant for PHENCYCLIDINE EIA ASSAY, MODIFICATION?

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

What is the FDA product code for PHENCYCLIDINE EIA ASSAY, MODIFICATION?

The FDA product code for PHENCYCLIDINE EIA ASSAY, MODIFICATION is LCM.

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Other records listing Diagnostic Reagents, Inc. as applicant

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Related Devices (Code: LCM)

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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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