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FDA 510(k)

VITAMIN B12 RADIOASSAY

K-Number: K780799 · 1978-06-13

ApplicantAmersham Corp.
Decision Date1978-06-13
Product CodeCDD
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

VITAMIN B12 RADIOASSAY is the device name listed in this FDA 510(k) record. The listed applicant is Amersham Corp.. It received FDA 510(k) clearance on 1978-06-13 under 510(k) number K780799. 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 RADIOASSAY?

VITAMIN B12 RADIOASSAY is a medical device that received FDA 510(k) clearance on 1978-06-13. The listed applicant is Amersham Corp.. The 510(k) number is K780799.

When did VITAMIN B12 RADIOASSAY receive FDA 510(k) clearance?

VITAMIN B12 RADIOASSAY received FDA 510(k) clearance on 1978-06-13, under 510(k) number K780799.

Who is the listed applicant for VITAMIN B12 RADIOASSAY?

The FDA 510(k) record lists Amersham Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VITAMIN B12 RADIOASSAY?

The FDA product code for VITAMIN B12 RADIOASSAY is CDD.

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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.

K233541ARCHITECT Active-B12 (Holotranscobalamin)Axis-Shield Diagnostics, Ltd.K223289Access Vitamin B12Beckman Coulter, Inc.K190298DxA 5000, DxI 800 Access Immunoassay System, Access Ferritin, Access Folate, Access TSH (3rd IS), Access Vitamin B12Beckman Coulter Biomedical GmbHK192064LIAISON Vitamin B12DiaSorin, Inc.K172133ADVIA Centaur Active-B12 (Holotranscobalamin) (AB12) AssayAxis-Shield Diagnostics, Ltd.K161721Diazyme Vitamin B12 Assay, Diazyme Vitamin B12 Calibrators Set, Diazyme Vitamin B12 Controls SetDiazyme Laboratories

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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