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FDA 510(k)

DRUG MIXTURE CONTROL IN URINE

K-Number: K880512 · 1988-04-05

Decision Date1988-04-05
Product CodeDIF
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

DRUG MIXTURE CONTROL IN URINE is the device name listed in this FDA 510(k) record. The listed applicant is Eastern Laboratories, Ltd.. It received FDA 510(k) clearance on 1988-04-05 under 510(k) number K880512. The device is classified under product code DIF. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DRUG MIXTURE CONTROL IN URINE?

DRUG MIXTURE CONTROL IN URINE is a medical device that received FDA 510(k) clearance on 1988-04-05. The listed applicant is Eastern Laboratories, Ltd.. The 510(k) number is K880512.

When did DRUG MIXTURE CONTROL IN URINE receive FDA 510(k) clearance?

DRUG MIXTURE CONTROL IN URINE received FDA 510(k) clearance on 1988-04-05, under 510(k) number K880512.

Who is the listed applicant for DRUG MIXTURE CONTROL IN URINE?

The FDA 510(k) record lists Eastern Laboratories, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DRUG MIXTURE CONTROL IN URINE?

The FDA product code for DRUG MIXTURE CONTROL IN URINE is DIF.

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 Eastern Laboratories, Ltd. 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.

Related Devices (Code: DIF)

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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