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FDA 510(k)

VENTREX COATED TUBE T3 UPTAKE

K-Number: K891068 · 1989-04-10

ApplicantVentrex Laboratories, Inc.
Decision Date1989-04-10
Product CodeKHQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

VENTREX COATED TUBE T3 UPTAKE 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 1989-04-10 under 510(k) number K891068. The device is classified under product code KHQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VENTREX COATED TUBE T3 UPTAKE?

VENTREX COATED TUBE T3 UPTAKE is a medical device that received FDA 510(k) clearance on 1989-04-10. The listed applicant is Ventrex Laboratories, Inc.. The 510(k) number is K891068.

When did VENTREX COATED TUBE T3 UPTAKE receive FDA 510(k) clearance?

VENTREX COATED TUBE T3 UPTAKE received FDA 510(k) clearance on 1989-04-10, under 510(k) number K891068.

Who is the listed applicant for VENTREX COATED TUBE T3 UPTAKE?

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 T3 UPTAKE?

The FDA product code for VENTREX COATED TUBE T3 UPTAKE is KHQ.

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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: KHQ)

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.

K981375ACE T UPTAKE REAGENT TU CALIBRATORSSchiapparelli Biosystems, Inc.K980088T-UPTAKE MICROPLATE EIAMonobindK970539CHIRON DIAGNOSTICS ACS:180TU PChiron Diagnostics Corp.K964308VITROS IMMUNODIAGNOSTICS PRODUCTS T3 UPTAKE REAGENT PACK (GEM.1025) AND T3 UPTAKE CALIBRATORS (GEM.C025)Johnson & Johnson Clinical Diagnostics, Inc.K961488ELECSYS T-UPTAKE ASSAYBoehringer Mannheim Corp.K954807CEDIA T UPTAKE ASSAYBoehringer Mannheim Corp.

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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