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FDA 510(k)

COCKSACKIEVIRUS B6 MONOCLONAL ANTIBODY

K-Number: K936254 · 1995-09-08

Decision Date1995-09-08
Product CodeGNM
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

COCKSACKIEVIRUS B6 MONOCLONAL ANTIBODY is the device name listed in this FDA 510(k) record. The listed applicant is Light Diagnostics. It received FDA 510(k) clearance on 1995-09-08 under 510(k) number K936254. The device is classified under product code GNM. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COCKSACKIEVIRUS B6 MONOCLONAL ANTIBODY?

COCKSACKIEVIRUS B6 MONOCLONAL ANTIBODY is a medical device that received FDA 510(k) clearance on 1995-09-08. The listed applicant is Light Diagnostics. The 510(k) number is K936254.

When did COCKSACKIEVIRUS B6 MONOCLONAL ANTIBODY receive FDA 510(k) clearance?

COCKSACKIEVIRUS B6 MONOCLONAL ANTIBODY received FDA 510(k) clearance on 1995-09-08, under 510(k) number K936254.

Who is the listed applicant for COCKSACKIEVIRUS B6 MONOCLONAL ANTIBODY?

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

What is the FDA product code for COCKSACKIEVIRUS B6 MONOCLONAL ANTIBODY?

The FDA product code for COCKSACKIEVIRUS B6 MONOCLONAL ANTIBODY is GNM.

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 Light Diagnostics 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 19 devices →

Related Devices (Code: GNM)

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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