BMC RF CANNULA
K-Number: K972846 · 1998-07-17
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Device Summary
Frequently Asked Questions
What is the BMC RF CANNULA?
BMC RF CANNULA is a medical device that received FDA 510(k) clearance on 1998-07-17. The listed applicant is Baylis Medical Co., Inc.. The 510(k) number is K972846.
When did BMC RF CANNULA receive FDA 510(k) clearance?
BMC RF CANNULA received FDA 510(k) clearance on 1998-07-17, under 510(k) number K972846.
Who is the listed applicant for BMC RF CANNULA?
The FDA 510(k) record lists Baylis Medical Co., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BMC RF CANNULA?
The FDA product code for BMC RF CANNULA is GXI.
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 Baylis Medical Co., 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: GXI)
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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