MERCURY MEDICAL DISPOSABLE RADIOFREQUENCY CANNULA
K-Number: K000073 · 2000-03-01
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Device Summary
Frequently Asked Questions
What is the MERCURY MEDICAL DISPOSABLE RADIOFREQUENCY CANNULA?
MERCURY MEDICAL DISPOSABLE RADIOFREQUENCY CANNULA is a medical device that received FDA 510(k) clearance on 2000-03-01. The listed applicant is Mercury Medical. The 510(k) number is K000073.
When did MERCURY MEDICAL DISPOSABLE RADIOFREQUENCY CANNULA receive FDA 510(k) clearance?
MERCURY MEDICAL DISPOSABLE RADIOFREQUENCY CANNULA received FDA 510(k) clearance on 2000-03-01, under 510(k) number K000073.
Who is the listed applicant for MERCURY MEDICAL DISPOSABLE RADIOFREQUENCY CANNULA?
The FDA 510(k) record lists Mercury Medical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MERCURY MEDICAL DISPOSABLE RADIOFREQUENCY CANNULA?
The FDA product code for MERCURY MEDICAL DISPOSABLE RADIOFREQUENCY 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 Mercury Medical 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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