VARELISA DSDNA ANTIBODIES (FARR VERSION)
K-Number: K950031 · 1995-03-10
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Device Summary
Frequently Asked Questions
What is the VARELISA DSDNA ANTIBODIES (FARR VERSION)?
VARELISA DSDNA ANTIBODIES (FARR VERSION) is a medical device that received FDA 510(k) clearance on 1995-03-10. The listed applicant is Elias U.S.A., Inc.. The 510(k) number is K950031.
When did VARELISA DSDNA ANTIBODIES (FARR VERSION) receive FDA 510(k) clearance?
VARELISA DSDNA ANTIBODIES (FARR VERSION) received FDA 510(k) clearance on 1995-03-10, under 510(k) number K950031.
Who is the listed applicant for VARELISA DSDNA ANTIBODIES (FARR VERSION)?
The FDA 510(k) record lists Elias U.S.A., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VARELISA DSDNA ANTIBODIES (FARR VERSION)?
The FDA product code for VARELISA DSDNA ANTIBODIES (FARR VERSION) is LRM.
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 Elias U.S.A., Inc. 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: LRM)
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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