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FDA 510(k)

TANDEM-M IMMUNOENZYMETRIC ASSAY FOR THYR/STIM/HORM

K-Number: K863859 · 1986-11-21

ApplicantHybritech, Inc.
Decision Date1986-11-21
Product CodeJLW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

TANDEM-M IMMUNOENZYMETRIC ASSAY FOR THYR/STIM/HORM is the device name listed in this FDA 510(k) record. The listed applicant is Hybritech, Inc.. It received FDA 510(k) clearance on 1986-11-21 under 510(k) number K863859. 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-M IMMUNOENZYMETRIC ASSAY FOR THYR/STIM/HORM?

TANDEM-M IMMUNOENZYMETRIC ASSAY FOR THYR/STIM/HORM is a medical device that received FDA 510(k) clearance on 1986-11-21. The listed applicant is Hybritech, Inc.. The 510(k) number is K863859.

When did TANDEM-M IMMUNOENZYMETRIC ASSAY FOR THYR/STIM/HORM receive FDA 510(k) clearance?

TANDEM-M IMMUNOENZYMETRIC ASSAY FOR THYR/STIM/HORM received FDA 510(k) clearance on 1986-11-21, under 510(k) number K863859.

Who is the listed applicant for TANDEM-M IMMUNOENZYMETRIC ASSAY FOR THYR/STIM/HORM?

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-M IMMUNOENZYMETRIC ASSAY FOR THYR/STIM/HORM?

The FDA product code for TANDEM-M IMMUNOENZYMETRIC ASSAY FOR THYR/STIM/HORM 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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