DIAMEDIX IS-HSV 1&2 IGM TEST SYSTEM
K-Number: K002262 · 2000-11-28
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Device Summary
Frequently Asked Questions
What is the DIAMEDIX IS-HSV 1&2 IGM TEST SYSTEM?
DIAMEDIX IS-HSV 1&2 IGM TEST SYSTEM is a medical device that received FDA 510(k) clearance on 2000-11-28. The listed applicant is Diamedix Corp.. The 510(k) number is K002262.
When did DIAMEDIX IS-HSV 1&2 IGM TEST SYSTEM receive FDA 510(k) clearance?
DIAMEDIX IS-HSV 1&2 IGM TEST SYSTEM received FDA 510(k) clearance on 2000-11-28, under 510(k) number K002262.
Who is the listed applicant for DIAMEDIX IS-HSV 1&2 IGM TEST SYSTEM?
The FDA 510(k) record lists Diamedix Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DIAMEDIX IS-HSV 1&2 IGM TEST SYSTEM?
The FDA product code for DIAMEDIX IS-HSV 1&2 IGM TEST SYSTEM is LGC.
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 Diamedix Corp. 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.
Related Devices (Code: LGC)
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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