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FDA 510(k)

HTSH NEONATE RIA DIAGNOSTIC KIT

K-Number: K791747 · 1979-11-13

ApplicantAbbott Laboratories
Decision Date1979-11-13
Product CodeJLW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

HTSH NEONATE RIA DIAGNOSTIC KIT is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1979-11-13 under 510(k) number K791747. 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 HTSH NEONATE RIA DIAGNOSTIC KIT?

HTSH NEONATE RIA DIAGNOSTIC KIT is a medical device that received FDA 510(k) clearance on 1979-11-13. The listed applicant is Abbott Laboratories. The 510(k) number is K791747.

When did HTSH NEONATE RIA DIAGNOSTIC KIT receive FDA 510(k) clearance?

HTSH NEONATE RIA DIAGNOSTIC KIT received FDA 510(k) clearance on 1979-11-13, under 510(k) number K791747.

Who is the listed applicant for HTSH NEONATE RIA DIAGNOSTIC KIT?

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

What is the FDA product code for HTSH NEONATE RIA DIAGNOSTIC KIT?

The FDA product code for HTSH NEONATE RIA DIAGNOSTIC KIT is JLW.

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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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