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FDA 510(k)

VIRASTAT(R) FITC-LABEL ANTI-PARAINFLU 1,2&3 MONO ANT

K-Number: K933575 · 1994-11-28

ApplicantSymex Corp.
Decision Date1994-11-28
Product CodeGQP
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

VIRASTAT(R) FITC-LABEL ANTI-PARAINFLU 1,2&3 MONO ANT is the device name listed in this FDA 510(k) record. The listed applicant is Symex Corp.. It received FDA 510(k) clearance on 1994-11-28 under 510(k) number K933575. The device is classified under product code GQP. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIRASTAT(R) FITC-LABEL ANTI-PARAINFLU 1,2&3 MONO ANT?

VIRASTAT(R) FITC-LABEL ANTI-PARAINFLU 1,2&3 MONO ANT is a medical device that received FDA 510(k) clearance on 1994-11-28. The listed applicant is Symex Corp.. The 510(k) number is K933575.

When did VIRASTAT(R) FITC-LABEL ANTI-PARAINFLU 1,2&3 MONO ANT receive FDA 510(k) clearance?

VIRASTAT(R) FITC-LABEL ANTI-PARAINFLU 1,2&3 MONO ANT received FDA 510(k) clearance on 1994-11-28, under 510(k) number K933575.

Who is the listed applicant for VIRASTAT(R) FITC-LABEL ANTI-PARAINFLU 1,2&3 MONO ANT?

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

What is the FDA product code for VIRASTAT(R) FITC-LABEL ANTI-PARAINFLU 1,2&3 MONO ANT?

The FDA product code for VIRASTAT(R) FITC-LABEL ANTI-PARAINFLU 1,2&3 MONO ANT is GQP.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Related Devices (Code: GQP)

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.

K981226IMAGEARAINFLUENZA VIRUS GROUP (TYPES 1,2 AND 3) TEST AND IMAGEN PARAINFLUENZA VIRUS TEST TYPES 1,2 AND 3Dako Diagnostics , Ltd.

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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