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FDA 510(k)

HUMAN LUNG DIPLOID CELLS-MRC-5

K-Number: K934244 · 1994-01-03

ApplicantAdvanced Clinical Diagnostics
Decision Date1994-01-03
Product CodeKIR
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

HUMAN LUNG DIPLOID CELLS-MRC-5 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 1994-01-03 under 510(k) number K934244. The device is classified under product code KIR. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HUMAN LUNG DIPLOID CELLS-MRC-5?

HUMAN LUNG DIPLOID CELLS-MRC-5 is a medical device that received FDA 510(k) clearance on 1994-01-03. The listed applicant is Advanced Clinical Diagnostics. The 510(k) number is K934244.

When did HUMAN LUNG DIPLOID CELLS-MRC-5 receive FDA 510(k) clearance?

HUMAN LUNG DIPLOID CELLS-MRC-5 received FDA 510(k) clearance on 1994-01-03, under 510(k) number K934244.

Who is the listed applicant for HUMAN LUNG DIPLOID CELLS-MRC-5?

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 HUMAN LUNG DIPLOID CELLS-MRC-5?

The FDA product code for HUMAN LUNG DIPLOID CELLS-MRC-5 is KIR.

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Other records listing Advanced Clinical Diagnostics as applicant

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Related Devices (Code: KIR)

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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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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