C & B 45
K-Number: K833278 · 1983-12-29
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Device Summary
Frequently Asked Questions
What is the C & B 45?
C & B 45 is a medical device that received FDA 510(k) clearance on 1983-12-29. The listed applicant is Genesis Industries, Inc.. The 510(k) number is K833278.
When did C & B 45 receive FDA 510(k) clearance?
C & B 45 received FDA 510(k) clearance on 1983-12-29, under 510(k) number K833278.
Who is the listed applicant for C & B 45?
The FDA 510(k) record lists Genesis Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for C & B 45?
The FDA product code for C & B 45 is EIS.
Other records listing Genesis Industries, 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: EIS)
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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