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)

CAVITRON ULTRASONIC SURG. ASPIR. CUSA

K-Number: K801623 · 1980-11-18

ApplicantCavitron Corp.
Decision Date1980-11-18
Product CodeLFL
DecisionSubstantially Equivalent

Device Summary

CAVITRON ULTRASONIC SURG. ASPIR. CUSA is the device name listed in this FDA 510(k) record. The listed applicant is Cavitron Corp.. It received FDA 510(k) clearance on 1980-11-18 under 510(k) number K801623. The device is classified under product code LFL. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAVITRON ULTRASONIC SURG. ASPIR. CUSA?

CAVITRON ULTRASONIC SURG. ASPIR. CUSA is a medical device that received FDA 510(k) clearance on 1980-11-18. The listed applicant is Cavitron Corp.. The 510(k) number is K801623.

When did CAVITRON ULTRASONIC SURG. ASPIR. CUSA receive FDA 510(k) clearance?

CAVITRON ULTRASONIC SURG. ASPIR. CUSA received FDA 510(k) clearance on 1980-11-18, under 510(k) number K801623.

Who is the listed applicant for CAVITRON ULTRASONIC SURG. ASPIR. CUSA?

The FDA 510(k) record lists Cavitron Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CAVITRON ULTRASONIC SURG. ASPIR. CUSA?

The FDA product code for CAVITRON ULTRASONIC SURG. ASPIR. CUSA 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 Cavitron Corp. 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.

K811582THE PLACERK810207MINOR SURGERY LIGHTK802928SPIROMETRIC COMPUTER #SC-10K801877SLIT LAMP ATTACHMENTK800869MODEL PM-20(N)(R)CO2 PATIENT MONITOR/ALAK800722AUTO-FIELD D AUTOMATED VISUAL DETECTOR

View all 32 devices →

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.

↑