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FDA 510(k)

PHOSPHORUS-SL ASSAY, CATALOGUE NUMBER 117-10, 117-30

K-Number: K974858 · 1998-01-30

ApplicantDiagnostic Chemicals , Ltd.
Decision Date1998-01-30
Product CodeCEO
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

PHOSPHORUS-SL ASSAY, CATALOGUE NUMBER 117-10, 117-30 is the device name listed in this FDA 510(k) record. The listed applicant is Diagnostic Chemicals , Ltd.. It received FDA 510(k) clearance on 1998-01-30 under 510(k) number K974858. The device is classified under product code CEO. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHOSPHORUS-SL ASSAY, CATALOGUE NUMBER 117-10, 117-30?

PHOSPHORUS-SL ASSAY, CATALOGUE NUMBER 117-10, 117-30 is a medical device that received FDA 510(k) clearance on 1998-01-30. The listed applicant is Diagnostic Chemicals , Ltd.. The 510(k) number is K974858.

When did PHOSPHORUS-SL ASSAY, CATALOGUE NUMBER 117-10, 117-30 receive FDA 510(k) clearance?

PHOSPHORUS-SL ASSAY, CATALOGUE NUMBER 117-10, 117-30 received FDA 510(k) clearance on 1998-01-30, under 510(k) number K974858.

Who is the listed applicant for PHOSPHORUS-SL ASSAY, CATALOGUE NUMBER 117-10, 117-30?

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

What is the FDA product code for PHOSPHORUS-SL ASSAY, CATALOGUE NUMBER 117-10, 117-30?

The FDA product code for PHOSPHORUS-SL ASSAY, CATALOGUE NUMBER 117-10, 117-30 is CEO.

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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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