TRISEDTA-BORATE ELECTROPHORESIS FILM AGA
K-Number: K790943 · 1979-06-22
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Device Summary
Frequently Asked Questions
What is the TRISEDTA-BORATE ELECTROPHORESIS FILM AGA?
TRISEDTA-BORATE ELECTROPHORESIS FILM AGA is a medical device that received FDA 510(k) clearance on 1979-06-22. The listed applicant is Corning Medical & Scientific. The 510(k) number is K790943.
When did TRISEDTA-BORATE ELECTROPHORESIS FILM AGA receive FDA 510(k) clearance?
TRISEDTA-BORATE ELECTROPHORESIS FILM AGA received FDA 510(k) clearance on 1979-06-22, under 510(k) number K790943.
Who is the listed applicant for TRISEDTA-BORATE ELECTROPHORESIS FILM AGA?
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 TRISEDTA-BORATE ELECTROPHORESIS FILM AGA?
The FDA product code for TRISEDTA-BORATE ELECTROPHORESIS FILM AGA is GHS.
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: GHS)
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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