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FDA 510(k)

LABELING CHANGE CANNABINOIDS DOUBLE ANTI. IN URINE

K-Number: K873753 · 1987-10-15

ApplicantDiagnostic Products Corp.
Decision Date1987-10-15
Product CodeLDJ
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

LABELING CHANGE CANNABINOIDS DOUBLE ANTI. IN URINE is the device name listed in this FDA 510(k) record. The listed applicant is Diagnostic Products Corp.. It received FDA 510(k) clearance on 1987-10-15 under 510(k) number K873753. 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 LABELING CHANGE CANNABINOIDS DOUBLE ANTI. IN URINE?

LABELING CHANGE CANNABINOIDS DOUBLE ANTI. IN URINE is a medical device that received FDA 510(k) clearance on 1987-10-15. The listed applicant is Diagnostic Products Corp.. The 510(k) number is K873753.

When did LABELING CHANGE CANNABINOIDS DOUBLE ANTI. IN URINE receive FDA 510(k) clearance?

LABELING CHANGE CANNABINOIDS DOUBLE ANTI. IN URINE received FDA 510(k) clearance on 1987-10-15, under 510(k) number K873753.

Who is the listed applicant for LABELING CHANGE CANNABINOIDS DOUBLE ANTI. IN URINE?

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

What is the FDA product code for LABELING CHANGE CANNABINOIDS DOUBLE ANTI. IN URINE?

The FDA product code for LABELING CHANGE CANNABINOIDS DOUBLE ANTI. IN URINE is LDJ.

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Other records listing Diagnostic Products Corp. as applicant

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Related Devices (Code: LDJ)

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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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