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FDA 510(k)

PHOSPHORUS (INORGANIC) TEST SYSTEM

K-Number: K910296 · 1991-02-27

Decision Date1991-02-27
Product CodeCEO
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

PHOSPHORUS (INORGANIC) TEST SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Biochemical Trade, Inc.. It received FDA 510(k) clearance on 1991-02-27 under 510(k) number K910296. 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 (INORGANIC) TEST SYSTEM?

PHOSPHORUS (INORGANIC) TEST SYSTEM is a medical device that received FDA 510(k) clearance on 1991-02-27. The listed applicant is Biochemical Trade, Inc.. The 510(k) number is K910296.

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

PHOSPHORUS (INORGANIC) TEST SYSTEM received FDA 510(k) clearance on 1991-02-27, under 510(k) number K910296.

Who is the listed applicant for PHOSPHORUS (INORGANIC) TEST SYSTEM?

The FDA 510(k) record lists Biochemical Trade, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PHOSPHORUS (INORGANIC) TEST SYSTEM?

The FDA product code for PHOSPHORUS (INORGANIC) TEST SYSTEM is CEO.

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 Biochemical Trade, Inc. 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 20 devices →

Related Devices (Code: CEO)

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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