STARION INSTRUMENTS POWER POINT CAUTERY CLAMP
K-Number: K001273 · 2000-06-14
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Device Summary
Frequently Asked Questions
What is the STARION INSTRUMENTS POWER POINT CAUTERY CLAMP?
STARION INSTRUMENTS POWER POINT CAUTERY CLAMP is a medical device that received FDA 510(k) clearance on 2000-06-14. The listed applicant is Starion Instruments. The 510(k) number is K001273.
When did STARION INSTRUMENTS POWER POINT CAUTERY CLAMP receive FDA 510(k) clearance?
STARION INSTRUMENTS POWER POINT CAUTERY CLAMP received FDA 510(k) clearance on 2000-06-14, under 510(k) number K001273.
Who is the listed applicant for STARION INSTRUMENTS POWER POINT CAUTERY CLAMP?
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 STARION INSTRUMENTS POWER POINT CAUTERY CLAMP?
The FDA product code for STARION INSTRUMENTS POWER POINT CAUTERY CLAMP is GEI.
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: GEI)
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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