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FDA 510(k)

ACCUWELL TSH, MODEL KAW-TSH-960

K-Number: K001455 · 2000-11-02

ApplicantNeometrics, Inc.
Decision Date2000-11-02
Product CodeJLW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ACCUWELL TSH, MODEL KAW-TSH-960 is the device name listed in this FDA 510(k) record. The listed applicant is Neometrics, Inc.. It received FDA 510(k) clearance on 2000-11-02 under 510(k) number K001455. 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 ACCUWELL TSH, MODEL KAW-TSH-960?

ACCUWELL TSH, MODEL KAW-TSH-960 is a medical device that received FDA 510(k) clearance on 2000-11-02. The listed applicant is Neometrics, Inc.. The 510(k) number is K001455.

When did ACCUWELL TSH, MODEL KAW-TSH-960 receive FDA 510(k) clearance?

ACCUWELL TSH, MODEL KAW-TSH-960 received FDA 510(k) clearance on 2000-11-02, under 510(k) number K001455.

Who is the listed applicant for ACCUWELL TSH, MODEL KAW-TSH-960?

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 ACCUWELL TSH, MODEL KAW-TSH-960?

The FDA product code for ACCUWELL TSH, MODEL KAW-TSH-960 is JLW.

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Related Devices (Code: JLW)

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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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