CITRATE AGAR GEL AND BUFFER SET
K-Number: K790944 · 1979-06-28
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Device Summary
Frequently Asked Questions
What is the CITRATE AGAR GEL AND BUFFER SET?
CITRATE AGAR GEL AND BUFFER SET is a medical device that received FDA 510(k) clearance on 1979-06-28. The listed applicant is Corning Medical & Scientific. The 510(k) number is K790944.
When did CITRATE AGAR GEL AND BUFFER SET receive FDA 510(k) clearance?
CITRATE AGAR GEL AND BUFFER SET received FDA 510(k) clearance on 1979-06-28, under 510(k) number K790944.
Who is the listed applicant for CITRATE AGAR GEL AND BUFFER SET?
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 CITRATE AGAR GEL AND BUFFER SET?
The FDA product code for CITRATE AGAR GEL AND BUFFER SET is JBD.
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: JBD)
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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