ELECTROPHORESIS CONTROLS-3 IN 1
K-Number: K831263 · 1983-07-07
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Device Summary
Frequently Asked Questions
What is the ELECTROPHORESIS CONTROLS-3 IN 1?
ELECTROPHORESIS CONTROLS-3 IN 1 is a medical device that received FDA 510(k) clearance on 1983-07-07. The listed applicant is Corning Medical & Scientific. The 510(k) number is K831263.
When did ELECTROPHORESIS CONTROLS-3 IN 1 receive FDA 510(k) clearance?
ELECTROPHORESIS CONTROLS-3 IN 1 received FDA 510(k) clearance on 1983-07-07, under 510(k) number K831263.
Who is the listed applicant for ELECTROPHORESIS CONTROLS-3 IN 1?
The FDA 510(k) record lists Corning Medical & Scientific as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ELECTROPHORESIS CONTROLS-3 IN 1?
The FDA product code for ELECTROPHORESIS CONTROLS-3 IN 1 is JJY.
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 Corning Medical & Scientific 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: JJY)
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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