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)

SONOCA III

K-Number: K942095 · 1994-11-09

ApplicantHoll Meditronics, Inc.
Decision Date1994-11-09
Product CodeLFL
DecisionSubstantially Equivalent

Device Summary

SONOCA III is the device name listed in this FDA 510(k) record. The listed applicant is Holl Meditronics, Inc.. It received FDA 510(k) clearance on 1994-11-09 under 510(k) number K942095. The device is classified under product code LFL. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SONOCA III?

SONOCA III is a medical device that received FDA 510(k) clearance on 1994-11-09. The listed applicant is Holl Meditronics, Inc.. The 510(k) number is K942095.

When did SONOCA III receive FDA 510(k) clearance?

SONOCA III received FDA 510(k) clearance on 1994-11-09, under 510(k) number K942095.

Who is the listed applicant for SONOCA III?

The FDA 510(k) record lists Holl Meditronics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SONOCA III?

The FDA product code for SONOCA III is LFL.

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 Holl Meditronics, Inc. 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.

K954171ARCO-MBC, ARCO MCK911600ILCO INFRARED LIGHT COAGULATORK893924MOTO-MED RF-II AND PICOK901737SONOCA II ULTRASONIC SURGICAL DEVICEK893926SONOCA ULTRASONIC SURGICAL SYSTEM

Related Devices (Code: LFL)

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.

K261448neXus Ultrasonic Surgical Aspirator SystemMisonix, LLCK251162CUSA® Clarity Ultrasonic Surgical Aspirator SystemIntegra LifeSciences CorporationK242894SanAgile™ Ultrasonic Surgery Advanced Portable Controller (SA10); SanAgile™ Ultrasonic Surgery Advanced Dissector (SASD14); SanAgile™ Ultrasonic Surgery Advanced Dissector (SASD23); SanAgile™ Ultrasonic Surgery Advanced Dissector (SASD36); SanAgile™ Ultrasonic Surgery Advanced Dissector (SASD45)Shanghai Saints Sages Surgical Co., Ltd.K243930Sonopet iQ Ultrasonic Aspirator System (5500-050-000)Stryker InstrumentsK241700Tenex 2nd Generation SystemTrice Medical, Inc.K240493CUSA® Clarity Ultrasonic Surgical Aspirator SystemIntegra LifeSciences Corporation

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.

↑