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FDA 510(k)

CAUTERY GRASPER/DISSECTOR

K-Number: K994019 · 2000-01-20

ApplicantStarion Instruments
Decision Date2000-01-20
Product CodeHQP
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

CAUTERY GRASPER/DISSECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Starion Instruments. It received FDA 510(k) clearance on 2000-01-20 under 510(k) number K994019. The device is classified under product code HQP. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAUTERY GRASPER/DISSECTOR?

CAUTERY GRASPER/DISSECTOR is a medical device that received FDA 510(k) clearance on 2000-01-20. The listed applicant is Starion Instruments. The 510(k) number is K994019.

When did CAUTERY GRASPER/DISSECTOR receive FDA 510(k) clearance?

CAUTERY GRASPER/DISSECTOR received FDA 510(k) clearance on 2000-01-20, under 510(k) number K994019.

Who is the listed applicant for 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 CAUTERY GRASPER/DISSECTOR?

The FDA product code for 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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.

K070871STARION UNIVERSAL POWER SUPPLYK062257STARION INSTRUMENTS THERMAL LITIGATING SHEARSK050308THERMAL CAUTERY PROBEK043155STARION UNIVERSAL POWER SUPPLY (UPS)K002547STARION INSTRUMENTS POWER POINT CAUTERY GRASPER/DISSECTORK001273STARION INSTRUMENTS POWER POINT CAUTERY CLAMP

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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.

K121441CAUTERY; LOW TEMPERATURE (FINEADJUSTABLE FINE TIP, ELONGATED FINE TIP, MICRO FINE TIP)Bovie Medical CorporationK083428F7244, F7255, F7266, F7277, F7288, F7233, F7234 SERIES OF BATTERY-POWERED CAUTERYFiab SpaK062659KIRWAN DISPOSABLE BATTERY-POWERED CAUTERY, MODEL 41-61XX SERIESKirwan Surgical Products, Inc.K023506SURGICAL MEDICAL DEVICE CAUTERYModern Medical Equipment Mfg., Ltd.K002547STARION INSTRUMENTS POWER POINT CAUTERY GRASPER/DISSECTORStarion InstrumentsK990728THERMAL CAUTERY DEVICE, FORCEPSStarion Instruments

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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