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FDA 510(k)

CDT CYTOTOXI TEST

K-Number: K883560 · 1988-10-25

ApplicantAdvanced Clinical Diagnostics
Decision Date1988-10-25
Product CodeLLH
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

CDT CYTOTOXI TEST is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Clinical Diagnostics. It received FDA 510(k) clearance on 1988-10-25 under 510(k) number K883560. The device is classified under product code LLH. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CDT CYTOTOXI TEST?

CDT CYTOTOXI TEST is a medical device that received FDA 510(k) clearance on 1988-10-25. The listed applicant is Advanced Clinical Diagnostics. The 510(k) number is K883560.

When did CDT CYTOTOXI TEST receive FDA 510(k) clearance?

CDT CYTOTOXI TEST received FDA 510(k) clearance on 1988-10-25, under 510(k) number K883560.

Who is the listed applicant for CDT CYTOTOXI TEST?

The FDA 510(k) record lists Advanced Clinical Diagnostics as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CDT CYTOTOXI TEST?

The FDA product code for CDT CYTOTOXI TEST is LLH.

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Other records listing Advanced Clinical Diagnostics as applicant

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Related Devices (Code: LLH)

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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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