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FDA 510(k)

IMMUCHEM PRL-MW ELISA

K-Number: K922715 · 1992-10-05

Decision Date1992-10-05
Product CodeCFT
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

IMMUCHEM PRL-MW ELISA is the device name listed in this FDA 510(k) record. The listed applicant is Icn Biomedicals, Inc.. It received FDA 510(k) clearance on 1992-10-05 under 510(k) number K922715. The device is classified under product code CFT. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMMUCHEM PRL-MW ELISA?

IMMUCHEM PRL-MW ELISA is a medical device that received FDA 510(k) clearance on 1992-10-05. The listed applicant is Icn Biomedicals, Inc.. The 510(k) number is K922715.

When did IMMUCHEM PRL-MW ELISA receive FDA 510(k) clearance?

IMMUCHEM PRL-MW ELISA received FDA 510(k) clearance on 1992-10-05, under 510(k) number K922715.

Who is the listed applicant for IMMUCHEM PRL-MW ELISA?

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

What is the FDA product code for IMMUCHEM PRL-MW ELISA?

The FDA product code for IMMUCHEM PRL-MW ELISA is CFT.

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 Icn Biomedicals, 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 11 devices →

Related Devices (Code: CFT)

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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