ELECTRO IMMUNO ASSAY KIT
K-Number: K770150 · 1977-02-01
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Device Summary
Frequently Asked Questions
What is the ELECTRO IMMUNO ASSAY KIT?
ELECTRO IMMUNO ASSAY KIT is a medical device that received FDA 510(k) clearance on 1977-02-01. The listed applicant is Millipore Corp.. The 510(k) number is K770150.
When did ELECTRO IMMUNO ASSAY KIT receive FDA 510(k) clearance?
ELECTRO IMMUNO ASSAY KIT received FDA 510(k) clearance on 1977-02-01, under 510(k) number K770150.
Who is the listed applicant for ELECTRO IMMUNO ASSAY KIT?
The FDA 510(k) record lists Millipore Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ELECTRO IMMUNO ASSAY KIT?
The FDA product code for ELECTRO IMMUNO ASSAY KIT is JZS.
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 Millipore Corp. 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: JZS)
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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