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FDA 510(k)

RIALYZE VITAMIN B-12 TEST

K-Number: K781410 · 1978-09-27

Decision Date1978-09-27
Product CodeCDD
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

RIALYZE VITAMIN B-12 TEST is the device name listed in this FDA 510(k) record. The listed applicant is Ames Div., Miles Laboratories, Inc.. It received FDA 510(k) clearance on 1978-09-27 under 510(k) number K781410. 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 RIALYZE VITAMIN B-12 TEST?

RIALYZE VITAMIN B-12 TEST is a medical device that received FDA 510(k) clearance on 1978-09-27. The listed applicant is Ames Div., Miles Laboratories, Inc.. The 510(k) number is K781410.

When did RIALYZE VITAMIN B-12 TEST receive FDA 510(k) clearance?

RIALYZE VITAMIN B-12 TEST received FDA 510(k) clearance on 1978-09-27, under 510(k) number K781410.

Who is the listed applicant for RIALYZE VITAMIN B-12 TEST?

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

What is the FDA product code for RIALYZE VITAMIN B-12 TEST?

The FDA product code for RIALYZE VITAMIN B-12 TEST 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.

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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