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FDA 510(k)

CENTRIA T3 UPTAKE TEST SET

K-Number: K791050 · 1979-06-15

ApplicantVentrex Laboratories, Inc.
Decision Date1979-06-15
Product Code
DecisionSubstantially Equivalent

Device Summary

CENTRIA T3 UPTAKE TEST SET 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 1979-06-15 under 510(k) number K791050. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CENTRIA T3 UPTAKE TEST SET?

CENTRIA T3 UPTAKE TEST SET is a medical device that received FDA 510(k) clearance on 1979-06-15. The listed applicant is Ventrex Laboratories, Inc.. The 510(k) number is K791050.

When did CENTRIA T3 UPTAKE TEST SET receive FDA 510(k) clearance?

CENTRIA T3 UPTAKE TEST SET received FDA 510(k) clearance on 1979-06-15, under 510(k) number K791050.

Who is the listed applicant for CENTRIA T3 UPTAKE TEST SET?

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

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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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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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