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FDA 510(k)

RAICHEM ALKALINE PHOSPHATASE REAGENT

K-Number: K832463 · 1983-09-12

ApplicantReagents Applications, Inc.
Decision Date1983-09-12
Product CodeCJE
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

RAICHEM ALKALINE PHOSPHATASE REAGENT is the device name listed in this FDA 510(k) record. The listed applicant is Reagents Applications, Inc.. It received FDA 510(k) clearance on 1983-09-12 under 510(k) number K832463. 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 RAICHEM ALKALINE PHOSPHATASE REAGENT?

RAICHEM ALKALINE PHOSPHATASE REAGENT is a medical device that received FDA 510(k) clearance on 1983-09-12. The listed applicant is Reagents Applications, Inc.. The 510(k) number is K832463.

When did RAICHEM ALKALINE PHOSPHATASE REAGENT receive FDA 510(k) clearance?

RAICHEM ALKALINE PHOSPHATASE REAGENT received FDA 510(k) clearance on 1983-09-12, under 510(k) number K832463.

Who is the listed applicant for RAICHEM ALKALINE PHOSPHATASE REAGENT?

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

What is the FDA product code for RAICHEM ALKALINE PHOSPHATASE REAGENT?

The FDA product code for RAICHEM ALKALINE PHOSPHATASE REAGENT is CJE.

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Other records listing Reagents Applications, Inc. as applicant

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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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