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FDA 510(k)

CENTRIA VITAMIN B12 FOLATE RADIO SET

K-Number: K791216 · 1979-11-13

Decision Date1979-11-13
Product CodeCDD
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CENTRIA VITAMIN B12 FOLATE RADIO 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 1979-11-13 under 510(k) number K791216. The device is classified under product code CDD. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CENTRIA VITAMIN B12 FOLATE RADIO SET?

CENTRIA VITAMIN B12 FOLATE RADIO SET is a medical device that received FDA 510(k) clearance on 1979-11-13. The listed applicant is Ventrex Laboratories, Inc.. The 510(k) number is K791216.

When did CENTRIA VITAMIN B12 FOLATE RADIO SET receive FDA 510(k) clearance?

CENTRIA VITAMIN B12 FOLATE RADIO SET received FDA 510(k) clearance on 1979-11-13, under 510(k) number K791216.

Who is the listed applicant for CENTRIA VITAMIN B12 FOLATE RADIO SET?

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 CENTRIA VITAMIN B12 FOLATE RADIO SET?

The FDA product code for CENTRIA VITAMIN B12 FOLATE RADIO SET is CDD.

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.

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.

View all 82 devices →

Related Devices (Code: CDD)

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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