PHASE II B-12/FOLATE KIT
K-Number: K853224 · 1985-10-03
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Device Summary
Frequently Asked Questions
What is the PHASE II B-12/FOLATE KIT?
PHASE II B-12/FOLATE KIT is a medical device that received FDA 510(k) clearance on 1985-10-03. The listed applicant is Medical & Scientific Designs, Inc.. The 510(k) number is K853224.
When did PHASE II B-12/FOLATE KIT receive FDA 510(k) clearance?
PHASE II B-12/FOLATE KIT received FDA 510(k) clearance on 1985-10-03, under 510(k) number K853224.
Who is the listed applicant for PHASE II B-12/FOLATE KIT?
The FDA 510(k) record lists Medical & Scientific Designs, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PHASE II B-12/FOLATE KIT?
The FDA product code for PHASE II B-12/FOLATE KIT 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 Medical & Scientific Designs, 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.
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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