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FDA 510(k)

VENTREX COATED TUBE HIGH SENSITIVITY TSH

K-Number: K885157 · 1989-02-10

ApplicantVentrex Laboratories, Inc.
Decision Date1989-02-10
Product CodeJLW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

VENTREX COATED TUBE HIGH SENSITIVITY TSH is the device name listed in this FDA 510(k) record. The listed applicant is Ventrex Laboratories, Inc.. It received FDA 510(k) clearance on 1989-02-10 under 510(k) number K885157. 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 VENTREX COATED TUBE HIGH SENSITIVITY TSH?

VENTREX COATED TUBE HIGH SENSITIVITY TSH is a medical device that received FDA 510(k) clearance on 1989-02-10. The listed applicant is Ventrex Laboratories, Inc.. The 510(k) number is K885157.

When did VENTREX COATED TUBE HIGH SENSITIVITY TSH receive FDA 510(k) clearance?

VENTREX COATED TUBE HIGH SENSITIVITY TSH received FDA 510(k) clearance on 1989-02-10, under 510(k) number K885157.

Who is the listed applicant for VENTREX COATED TUBE HIGH SENSITIVITY TSH?

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

What is the FDA product code for VENTREX COATED TUBE HIGH SENSITIVITY TSH?

The FDA product code for VENTREX COATED TUBE HIGH SENSITIVITY TSH is JLW.

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Other records listing Ventrex Laboratories, 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.

K914554SPECIFIC IGE EIA-TURBO ASSAYK913833VENTREX ALLERGEN DISCK913434VENTREX COATED TUBE INTACT PTHK905612VENTREX COATED TUBE IGE RADIOIMMUNOASSAYK905636VENTREX COATED TUBE IGE ENZYME IMMUNOASSAYK905247SHBG IRMA KIT

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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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