IMMUCHEM PRL-MW ELISA
K-Number: K922715 · 1992-10-05
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Device Summary
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.
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
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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