STARION INSTRUMENTS POWER POINT CAUTERY GRASPER/DISSECTOR
K-Number: K002547 · 2000-10-20
Advertisement
Device Summary
Frequently Asked Questions
What is the STARION INSTRUMENTS POWER POINT CAUTERY GRASPER/DISSECTOR?
STARION INSTRUMENTS POWER POINT CAUTERY GRASPER/DISSECTOR is a medical device that received FDA 510(k) clearance on 2000-10-20. The listed applicant is Starion Instruments. The 510(k) number is K002547.
When did STARION INSTRUMENTS POWER POINT CAUTERY GRASPER/DISSECTOR receive FDA 510(k) clearance?
STARION INSTRUMENTS POWER POINT CAUTERY GRASPER/DISSECTOR received FDA 510(k) clearance on 2000-10-20, under 510(k) number K002547.
Who is the listed applicant for STARION INSTRUMENTS POWER POINT CAUTERY GRASPER/DISSECTOR?
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 GRASPER/DISSECTOR?
The FDA product code for STARION INSTRUMENTS POWER POINT CAUTERY GRASPER/DISSECTOR is HQP.
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: HQP)
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.
Advertisement