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FDA 510(k)

VMA BY COLUMN TEST

K-Number: K791837 · 1979-10-30

ApplicantBio-Rad
Decision Date1979-10-30
Product CodeCDF
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

VMA BY COLUMN TEST is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Rad. It received FDA 510(k) clearance on 1979-10-30 under 510(k) number K791837. The device is classified under product code CDF. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VMA BY COLUMN TEST?

VMA BY COLUMN TEST is a medical device that received FDA 510(k) clearance on 1979-10-30. The listed applicant is Bio-Rad. The 510(k) number is K791837.

When did VMA BY COLUMN TEST receive FDA 510(k) clearance?

VMA BY COLUMN TEST received FDA 510(k) clearance on 1979-10-30, under 510(k) number K791837.

Who is the listed applicant for VMA BY COLUMN TEST?

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

What is the FDA product code for VMA BY COLUMN TEST?

The FDA product code for VMA BY COLUMN TEST is CDF.

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Other records listing Bio-Rad 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.

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Related Devices (Code: CDF)

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.

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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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