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FDA 510(k)

ACCUSCREEN TSH

K-Number: K843281 · 1984-09-26

ApplicantNeometrics, Inc.
Decision Date1984-09-26
Product CodeJLW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ACCUSCREEN TSH is the device name listed in this FDA 510(k) record. The listed applicant is Neometrics, Inc.. It received FDA 510(k) clearance on 1984-09-26 under 510(k) number K843281. The device is classified under product code JLW. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACCUSCREEN TSH?

ACCUSCREEN TSH is a medical device that received FDA 510(k) clearance on 1984-09-26. The listed applicant is Neometrics, Inc.. The 510(k) number is K843281.

When did ACCUSCREEN TSH receive FDA 510(k) clearance?

ACCUSCREEN TSH received FDA 510(k) clearance on 1984-09-26, under 510(k) number K843281.

Who is the listed applicant for ACCUSCREEN TSH?

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

What is the FDA product code for ACCUSCREEN TSH?

The FDA product code for ACCUSCREEN TSH is JLW.

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Other records listing Neometrics, Inc. as applicant

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Related Devices (Code: JLW)

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.

K251543Atellica® IM TSH3-Ultra II (TSH3ULII)Siemens Healthcare Diagnostics, Inc.K243570Dimension LOCI Thyroid Stimulating Hormone Flex reagent cartridge (TSHL); Dimension LOCI Free Thyroxine Flex reagent cartridge (FT4L)Siemens Healthcare DiagnosticsK234091Maverick Diagnostic System TC1000; Maverick Test Panel A0.B0Genalyte, Inc.K233050ADVIA Centaur® TSH3-Ultra II (TSH3ULII)Siemens Healthcare Diagnostics, Inc.K222116Atellica® CI Analyzer, Atellica® IMThyroid Stimulating Hormone 3-Ultra (TSH3-UL), Atellica® CH Albumin BCP (AlbP)Siemens Healthcare Diagnostics, Inc.K221225Access TSH (3rd IS) Assay, DxI 9000 Access Immunoassay AnalyzerBeckman Coulter, Inc.

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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