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FDA 510(k)

ACID PHOSPHATASE TEST

K-Number: K873726 · 1988-01-27

ApplicantKing Diagnostics, Inc.
Decision Date1988-01-27
Product CodeCKE
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ACID PHOSPHATASE TEST is the device name listed in this FDA 510(k) record. The listed applicant is King Diagnostics, Inc.. It received FDA 510(k) clearance on 1988-01-27 under 510(k) number K873726. The device is classified under product code CKE. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACID PHOSPHATASE TEST?

ACID PHOSPHATASE TEST is a medical device that received FDA 510(k) clearance on 1988-01-27. The listed applicant is King Diagnostics, Inc.. The 510(k) number is K873726.

When did ACID PHOSPHATASE TEST receive FDA 510(k) clearance?

ACID PHOSPHATASE TEST received FDA 510(k) clearance on 1988-01-27, under 510(k) number K873726.

Who is the listed applicant for ACID PHOSPHATASE TEST?

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

What is the FDA product code for ACID PHOSPHATASE TEST?

The FDA product code for ACID PHOSPHATASE TEST is CKE.

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Other records listing King Diagnostics, 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.

K933329KING DIAGNOSTICS IRON AND TOTAL IRON BINDING CAPACITY REAGENTK931834KING SODIUM/POTASSIUM STANDARD MODIFIEDK931773HDL PRECIPITATING REAGENT (DEXTRAN SULFATE)K931326KING DIAGNOSTICS CK REAGENTK923129KING DIAGNOSTICS GLUCOSE (HK) REAGENTK922969KING DIAGNOSTICS UREA NITROGEN REAGENT

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Related Devices (Code: CKE)

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.

K914167CLINICAL CHEM.ANAL.ACID,PROSTATIC ACID PHOSPHATASEEastman Kodak CompanyK915705ACID PHOSPHATASE REAGENT SETTech Intl. Co.K864230DIMENSION (TM) CLINICAL CHEMISTRY SYSTEME.I. Dupont DE Nemours & Co., Inc.K860476ACID PHOSPHATASE REAGENT SETSterling Diagnostics, Inc.K843380ACID PHOSPHATASE ASSAY KITDiagnostic Chemicals, Ltd. (Usa)K821526ACID PHOSPHATASE REAGENT SETAnco Medical Reagents & Assoc.

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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