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FDA 510(k)

VITAMIN B12 - NO-BOIL KIT

K-Number: K801579 · 1980-10-23

Decision Date1980-10-23
Product CodeCDD
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

VITAMIN B12 - NO-BOIL KIT is the device name listed in this FDA 510(k) record. The listed applicant is Ria Products, Inc.. It received FDA 510(k) clearance on 1980-10-23 under 510(k) number K801579. 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 VITAMIN B12 - NO-BOIL KIT?

VITAMIN B12 - NO-BOIL KIT is a medical device that received FDA 510(k) clearance on 1980-10-23. The listed applicant is Ria Products, Inc.. The 510(k) number is K801579.

When did VITAMIN B12 - NO-BOIL KIT receive FDA 510(k) clearance?

VITAMIN B12 - NO-BOIL KIT received FDA 510(k) clearance on 1980-10-23, under 510(k) number K801579.

Who is the listed applicant for VITAMIN B12 - NO-BOIL KIT?

The FDA 510(k) record lists Ria Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VITAMIN B12 - NO-BOIL KIT?

The FDA product code for VITAMIN B12 - NO-BOIL 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 Ria Products, 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.

View all 9 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

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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