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FDA 510(k)

TANDEM-E THYROID STIMULATING HORMONE KIT

K-Number: K832813 · 1983-10-31

ApplicantHybritech, Inc.
Decision Date1983-10-31
Product CodeJLW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

TANDEM-E THYROID STIMULATING HORMONE KIT is the device name listed in this FDA 510(k) record. The listed applicant is Hybritech, Inc.. It received FDA 510(k) clearance on 1983-10-31 under 510(k) number K832813. 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 TANDEM-E THYROID STIMULATING HORMONE KIT?

TANDEM-E THYROID STIMULATING HORMONE KIT is a medical device that received FDA 510(k) clearance on 1983-10-31. The listed applicant is Hybritech, Inc.. The 510(k) number is K832813.

When did TANDEM-E THYROID STIMULATING HORMONE KIT receive FDA 510(k) clearance?

TANDEM-E THYROID STIMULATING HORMONE KIT received FDA 510(k) clearance on 1983-10-31, under 510(k) number K832813.

Who is the listed applicant for TANDEM-E THYROID STIMULATING HORMONE KIT?

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

What is the FDA product code for TANDEM-E THYROID STIMULATING HORMONE KIT?

The FDA product code for TANDEM-E THYROID STIMULATING HORMONE KIT is JLW.

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Other records listing Hybritech, 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.

K972666TANDEM-MP OSTASE IMMUNOENZYMETRIC ASSAYK961573TANDEM-R OSTASE IMMUNORADIOMETRIC ASSAYK930810TANDEM-R OSTASE IMMUNORADIOMETRIC ASSAYK922754TANDEM-E IGE II CALIBRATION VERIFICATION SETK921745HYBRITECH STRATUS PAP FLUOROMETRIC ENZYME IMMUNOK921252TANDEM-E FERRITIN CALIBRATION VERIFICATION CONROL

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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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