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FDA 510(k)

VARELISA RNP-SM ANTIBODIES

K-Number: K944167 · 1994-12-22

Decision Date1994-12-22
Product CodeLJM
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

VARELISA RNP-SM ANTIBODIES is the device name listed in this FDA 510(k) record. The listed applicant is Elias U.S.A., Inc.. It received FDA 510(k) clearance on 1994-12-22 under 510(k) number K944167. The device is classified under product code LJM. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VARELISA RNP-SM ANTIBODIES?

VARELISA RNP-SM ANTIBODIES is a medical device that received FDA 510(k) clearance on 1994-12-22. The listed applicant is Elias U.S.A., Inc.. The 510(k) number is K944167.

When did VARELISA RNP-SM ANTIBODIES receive FDA 510(k) clearance?

VARELISA RNP-SM ANTIBODIES received FDA 510(k) clearance on 1994-12-22, under 510(k) number K944167.

Who is the listed applicant for VARELISA RNP-SM 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 VARELISA RNP-SM ANTIBODIES?

The FDA product code for VARELISA RNP-SM ANTIBODIES is LJM.

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.

View all 54 devices →

Related Devices (Code: LJM)

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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