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FDA 510(k)

CENTRIFICHEM INORGANIC PHOSPHORUS

K-Number: K790662 · 1979-05-15

Decision Date1979-05-15
Product CodeCED
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CENTRIFICHEM INORGANIC PHOSPHORUS is the device name listed in this FDA 510(k) record. The listed applicant is Union Carbide Corp.. It received FDA 510(k) clearance on 1979-05-15 under 510(k) number K790662. The device is classified under product code CED. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CENTRIFICHEM INORGANIC PHOSPHORUS?

CENTRIFICHEM INORGANIC PHOSPHORUS is a medical device that received FDA 510(k) clearance on 1979-05-15. The listed applicant is Union Carbide Corp.. The 510(k) number is K790662.

When did CENTRIFICHEM INORGANIC PHOSPHORUS receive FDA 510(k) clearance?

CENTRIFICHEM INORGANIC PHOSPHORUS received FDA 510(k) clearance on 1979-05-15, under 510(k) number K790662.

Who is the listed applicant for CENTRIFICHEM INORGANIC PHOSPHORUS?

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

What is the FDA product code for CENTRIFICHEM INORGANIC PHOSPHORUS?

The FDA product code for CENTRIFICHEM INORGANIC PHOSPHORUS is CED.

Related Clinical Trials

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.

Other records listing Union Carbide Corp. as applicant

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.

View all 69 devices →

Related Devices (Code: CED)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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