THERMAL CAUTERY PROBE
K-Number: K050308 · 2005-02-25
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Device Summary
Frequently Asked Questions
What is the THERMAL CAUTERY PROBE?
THERMAL CAUTERY PROBE is a medical device that received FDA 510(k) clearance on 2005-02-25. The listed applicant is Starion Instruments. The 510(k) number is K050308.
When did THERMAL CAUTERY PROBE receive FDA 510(k) clearance?
THERMAL CAUTERY PROBE received FDA 510(k) clearance on 2005-02-25, under 510(k) number K050308.
Who is the listed applicant for THERMAL CAUTERY PROBE?
The FDA 510(k) record lists Starion Instruments as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for THERMAL CAUTERY PROBE?
The FDA product code for THERMAL CAUTERY PROBE is HQR.
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 Starion Instruments 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: HQR)
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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