COAXIAL ELECTRODE #300A
K-Number: K832566 · 1983-11-28
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Device Summary
Frequently Asked Questions
What is the COAXIAL ELECTRODE #300A?
COAXIAL ELECTRODE #300A is a medical device that received FDA 510(k) clearance on 1983-11-28. The listed applicant is K-Med, Inc.. The 510(k) number is K832566.
When did COAXIAL ELECTRODE #300A receive FDA 510(k) clearance?
COAXIAL ELECTRODE #300A received FDA 510(k) clearance on 1983-11-28, under 510(k) number K832566.
Who is the listed applicant for COAXIAL ELECTRODE #300A?
The FDA 510(k) record lists K-Med, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for COAXIAL ELECTRODE #300A?
The FDA product code for COAXIAL ELECTRODE #300A is FFK.
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 K-Med, 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: FFK)
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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