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FDA 510(k)

DORN BLOOD CULTURE COLLECTION TUBE

K-Number: K791303 · 1979-09-17

Decision Date1979-09-17
Product CodeJKA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DORN BLOOD CULTURE COLLECTION TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Wadley Institutes of Molecular Medici. It received FDA 510(k) clearance on 1979-09-17 under 510(k) number K791303. The device is classified under product code JKA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DORN BLOOD CULTURE COLLECTION TUBE?

DORN BLOOD CULTURE COLLECTION TUBE is a medical device that received FDA 510(k) clearance on 1979-09-17. The listed applicant is Wadley Institutes of Molecular Medici. The 510(k) number is K791303.

When did DORN BLOOD CULTURE COLLECTION TUBE receive FDA 510(k) clearance?

DORN BLOOD CULTURE COLLECTION TUBE received FDA 510(k) clearance on 1979-09-17, under 510(k) number K791303.

Who is the listed applicant for DORN BLOOD CULTURE COLLECTION TUBE?

The FDA 510(k) record lists Wadley Institutes of Molecular Medici as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DORN BLOOD CULTURE COLLECTION TUBE?

The FDA product code for DORN BLOOD CULTURE COLLECTION TUBE is JKA.

Related Clinical Trials

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.

Related Devices (Code: JKA)

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.

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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