CBA FORMALIN
K-Number: K842940 · 1984-08-28
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Device Summary
Frequently Asked Questions
What is the CBA FORMALIN?
CBA FORMALIN is a medical device that received FDA 510(k) clearance on 1984-08-28. The listed applicant is Anatech, Ltd.. The 510(k) number is K842940.
When did CBA FORMALIN receive FDA 510(k) clearance?
CBA FORMALIN received FDA 510(k) clearance on 1984-08-28, under 510(k) number K842940.
Who is the listed applicant for CBA FORMALIN?
The FDA 510(k) record lists Anatech, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CBA FORMALIN?
The FDA product code for CBA FORMALIN is IFP.
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 Anatech, Ltd. 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: IFP)
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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