ELIAS CARDIOLIPIN IGG ANTIBODIES
K-Number: K933393 · 1993-12-08
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Device Summary
Frequently Asked Questions
What is the ELIAS CARDIOLIPIN IGG ANTIBODIES?
ELIAS CARDIOLIPIN IGG ANTIBODIES is a medical device that received FDA 510(k) clearance on 1993-12-08. The listed applicant is Elias U.S.A., Inc.. The 510(k) number is K933393.
When did ELIAS CARDIOLIPIN IGG ANTIBODIES receive FDA 510(k) clearance?
ELIAS CARDIOLIPIN IGG ANTIBODIES received FDA 510(k) clearance on 1993-12-08, under 510(k) number K933393.
Who is the listed applicant for ELIAS CARDIOLIPIN IGG ANTIBODIES?
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 ELIAS CARDIOLIPIN IGG ANTIBODIES?
The FDA product code for ELIAS CARDIOLIPIN IGG ANTIBODIES is MID.
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: MID)
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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