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FDA 510(k)

EMDS ALKALINE PHOSPHATASE (ALP) TEST

K-Number: K924574 · 1992-11-09

ApplicantEm Diagnostic Systems, Inc.
Decision Date1992-11-09
Product CodeCJE
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

EMDS ALKALINE PHOSPHATASE (ALP) TEST is the device name listed in this FDA 510(k) record. The listed applicant is Em Diagnostic Systems, Inc.. It received FDA 510(k) clearance on 1992-11-09 under 510(k) number K924574. The device is classified under product code CJE. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EMDS ALKALINE PHOSPHATASE (ALP) TEST?

EMDS ALKALINE PHOSPHATASE (ALP) TEST is a medical device that received FDA 510(k) clearance on 1992-11-09. The listed applicant is Em Diagnostic Systems, Inc.. The 510(k) number is K924574.

When did EMDS ALKALINE PHOSPHATASE (ALP) TEST receive FDA 510(k) clearance?

EMDS ALKALINE PHOSPHATASE (ALP) TEST received FDA 510(k) clearance on 1992-11-09, under 510(k) number K924574.

Who is the listed applicant for EMDS ALKALINE PHOSPHATASE (ALP) TEST?

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

What is the FDA product code for EMDS ALKALINE PHOSPHATASE (ALP) TEST?

The FDA product code for EMDS ALKALINE PHOSPHATASE (ALP) TEST is CJE.

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Other records listing Em Diagnostic Systems, 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.

K935181ASPARTATE AMINOTRANSFERASE (AST) TESTK935180ALANINE AMINOTRANSFERASE (ALT) TESTK935178EMDS PHOSPHOROUS (PHOS) TESTK935179EMDS ALBUMIN (ALB) TESTK935175LACTATE DEHYDROGENASE (LD)K935174TOTAL PROTEIN TEST (TPRO)

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Related Devices (Code: CJE)

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.

K251074Tru Liver Health Test PanelTruvian HealthK240468Alkaline PhosphataseAbbott Laboratories Diagnostics DivisionK223317Alkaline Phosphatase2Abbott Ireland Diagnostics DivisionK191245Yumizen C1200 ALP, Yumizen C1200 AlbuminHORIBA ABX SASK171971Comprehensive Metabolic Panel, skyla Clinical Chemistry Analyzer, Minicare C300 Clinical Chemistry AnalyzerLite-On Technology Corp. H.S.P.B.K171080ALP IFCC Gen.2Roche Diagnostics Operations (Rdo)

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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