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FDA 510(k)

INORGANIC PHOSPHORUS (IP), PRODUCT NO'S, 112-01, 112-02

K-Number: K991867 · 1999-08-02

ApplicantA.P. Total Care, Inc.
Decision Date1999-08-02
Product CodeCEO
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

INORGANIC PHOSPHORUS (IP), PRODUCT NO'S, 112-01, 112-02 is the device name listed in this FDA 510(k) record. The listed applicant is A.P. Total Care, Inc.. It received FDA 510(k) clearance on 1999-08-02 under 510(k) number K991867. 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 INORGANIC PHOSPHORUS (IP), PRODUCT NO'S, 112-01, 112-02?

INORGANIC PHOSPHORUS (IP), PRODUCT NO'S, 112-01, 112-02 is a medical device that received FDA 510(k) clearance on 1999-08-02. The listed applicant is A.P. Total Care, Inc.. The 510(k) number is K991867.

When did INORGANIC PHOSPHORUS (IP), PRODUCT NO'S, 112-01, 112-02 receive FDA 510(k) clearance?

INORGANIC PHOSPHORUS (IP), PRODUCT NO'S, 112-01, 112-02 received FDA 510(k) clearance on 1999-08-02, under 510(k) number K991867.

Who is the listed applicant for INORGANIC PHOSPHORUS (IP), PRODUCT NO'S, 112-01, 112-02?

The FDA 510(k) record lists A.P. Total Care, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INORGANIC PHOSPHORUS (IP), PRODUCT NO'S, 112-01, 112-02?

The FDA product code for INORGANIC PHOSPHORUS (IP), PRODUCT NO'S, 112-01, 112-02 is CEO.

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Other records listing A.P. Total Care, 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.

K991246FRUCTOSAMINE, MODEL FR 106-01K991761MAGNESIUM PRODUCT NO'S, 112-01, 112-02K991762ALKALINE PHOPHATASE (ALP), PRODUCT NO'S 118-01, 118-02K991664LDL CHOLESTEROL, PRODUCT NO'S, 124-01, CH102-01K991665HDL CHOLESTEROL, PRODUCT NO'S 124-01, CH102-01K991866BILIRUBIN, TOTAL AND DIRECT, PRODUCT NO, 122-01, 122-02, 122-03, 122-04

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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.

K100263ELITECH CLINICAL SYSTEMS PHOSPHORUS, URIC ACID MONO SL AND UREA UV SL REAGENTSSeppim S.A.S.K072141S40 CLINICAL ANALYZER, S TEST IP, S TEST UAAlfa Wassermann Diagnostic Technologies, Inc.K041643SYNCHRON SYSTEMS PHOSPHORUS (PHS) REAGENTBeckman Coulter, Inc.K030015ATAC PAK PHOSPHORUS REAGENTElan DiagnosticsK022312PICCOLO PHOSPHORUS TEST SYSTEMAbaxis, Inc.K013095WIENER LAB.FOSFATEMIA UV, MODELS 1X100 ML CAT.N 1382321, 4X20 ML CAT.N 1009311Wiener Laboratories Saic

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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