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FDA 510(k)

ELISA-DOXA SM/RNP

K-Number: K924948 · 1993-05-19

Decision Date1993-05-19
Product CodeLLL
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

ELISA-DOXA SM/RNP is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Biological Products, Inc.. It received FDA 510(k) clearance on 1993-05-19 under 510(k) number K924948. The device is classified under product code LLL. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELISA-DOXA SM/RNP?

ELISA-DOXA SM/RNP is a medical device that received FDA 510(k) clearance on 1993-05-19. The listed applicant is Advanced Biological Products, Inc.. The 510(k) number is K924948.

When did ELISA-DOXA SM/RNP receive FDA 510(k) clearance?

ELISA-DOXA SM/RNP received FDA 510(k) clearance on 1993-05-19, under 510(k) number K924948.

Who is the listed applicant for ELISA-DOXA SM/RNP?

The FDA 510(k) record lists Advanced Biological Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ELISA-DOXA SM/RNP?

The FDA product code for ELISA-DOXA SM/RNP is LLL.

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 Advanced Biological Products, 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 8 devices →

Related Devices (Code: LLL)

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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