RIALYZE VITAMIN B-12 TEST
K-Number: K781410 · 1978-09-27
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Device Summary
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
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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