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FDA 510(k)

NO BOIL DUAL COUNT VIT-B12 & FOLIC ACID

K-Number: K830195 · 1983-02-18

Decision Date1983-02-18
Product CodeCDD
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

NO BOIL DUAL COUNT VIT-B12 & FOLIC ACID is the device name listed in this FDA 510(k) record. The listed applicant is Diagnostic Products Corp.. It received FDA 510(k) clearance on 1983-02-18 under 510(k) number K830195. 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 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.

View all 321 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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