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FDA 510(k)

SERUM, INORGANIC PHOSPHOROUS

K-Number: K790021 · 1979-02-15

ApplicantFisher Scientific Co., LLC
Decision Date1979-02-15
Product CodeCEO
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SERUM, INORGANIC PHOSPHOROUS is the device name listed in this FDA 510(k) record. The listed applicant is Fisher Scientific Co., LLC. It received FDA 510(k) clearance on 1979-02-15 under 510(k) number K790021. 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 SERUM, INORGANIC PHOSPHOROUS?

SERUM, INORGANIC PHOSPHOROUS is a medical device that received FDA 510(k) clearance on 1979-02-15. The listed applicant is Fisher Scientific Co., LLC. The 510(k) number is K790021.

When did SERUM, INORGANIC PHOSPHOROUS receive FDA 510(k) clearance?

SERUM, INORGANIC PHOSPHOROUS received FDA 510(k) clearance on 1979-02-15, under 510(k) number K790021.

Who is the listed applicant for SERUM, INORGANIC PHOSPHOROUS?

The FDA 510(k) record lists Fisher Scientific Co., LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SERUM, INORGANIC PHOSPHOROUS?

The FDA product code for SERUM, INORGANIC PHOSPHOROUS is CEO.

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Other records listing Fisher Scientific Co., LLC as applicant

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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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