NO BOIL DUAL COUNT VIT-B12 & FOLIC ACID
K-Number: K830195 · 1983-02-18
Advertisement
Device Summary
Frequently Asked Questions
What is the NO BOIL DUAL COUNT VIT-B12 & FOLIC ACID?
NO BOIL DUAL COUNT VIT-B12 & FOLIC ACID is a medical device that received FDA 510(k) clearance on 1983-02-18. The listed applicant is Diagnostic Products Corp.. The 510(k) number is K830195.
When did NO BOIL DUAL COUNT VIT-B12 & FOLIC ACID receive FDA 510(k) clearance?
NO BOIL DUAL COUNT VIT-B12 & FOLIC ACID received FDA 510(k) clearance on 1983-02-18, under 510(k) number K830195.
Who is the listed applicant for NO BOIL DUAL COUNT VIT-B12 & FOLIC ACID?
The FDA 510(k) record lists Diagnostic Products Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NO BOIL DUAL COUNT VIT-B12 & FOLIC ACID?
The FDA product code for NO BOIL DUAL COUNT VIT-B12 & FOLIC ACID 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 Diagnostic Products Corp. 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.
Advertisement