Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

STARION UNIVERSAL POWER SUPPLY (UPS)

K-Number: K043155 · 2004-12-09

ApplicantStarion Instruments
Decision Date2004-12-09
Product CodeHQO
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

STARION UNIVERSAL POWER SUPPLY (UPS) is the device name listed in this FDA 510(k) record. The listed applicant is Starion Instruments. It received FDA 510(k) clearance on 2004-12-09 under 510(k) number K043155. The device is classified under product code HQO. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STARION UNIVERSAL POWER SUPPLY (UPS)?

STARION UNIVERSAL POWER SUPPLY (UPS) is a medical device that received FDA 510(k) clearance on 2004-12-09. The listed applicant is Starion Instruments. The 510(k) number is K043155.

When did STARION UNIVERSAL POWER SUPPLY (UPS) receive FDA 510(k) clearance?

STARION UNIVERSAL POWER SUPPLY (UPS) received FDA 510(k) clearance on 2004-12-09, under 510(k) number K043155.

Who is the listed applicant for STARION UNIVERSAL POWER SUPPLY (UPS)?

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 UNIVERSAL POWER SUPPLY (UPS)?

The FDA product code for STARION UNIVERSAL POWER SUPPLY (UPS) is HQO.

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 PROBEK002547STARION INSTRUMENTS POWER POINT CAUTERY GRASPER/DISSECTORK001262THERMAL CAUTERY FORCEPSK001273STARION INSTRUMENTS POWER POINT CAUTERY CLAMP

View all 13 devices →

Related Devices (Code: HQO)

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 SUPPLYStarion InstrumentsK002341THERMAL CAUTERY UNIT, MODEL 150Geiger Medical Technologies, Inc.K000893AC POWERED THERMAL CAUTERY UNITStarion InstrumentsK971538MENTOR GEMINI HEMOSTATIC ERASERMentor Ophthalmics, Inc.K962135D.O.R.C. MICRODIATHERMY SYSTEMDutch Ophthalmic USA, Inc.K943031BIPOLAR ELECTROSURGICAL PENCILBoston Surgical Products, Inc.

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.

↑