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)

LITHOVAC SUCTION/ASPIRATION PROBE

K-Number: K964111 · 1996-12-16

ApplicantElectro Medical Systems SA
Decision Date1996-12-16
Product CodeKQT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

LITHOVAC SUCTION/ASPIRATION PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Electro Medical Systems SA. It received FDA 510(k) clearance on 1996-12-16 under 510(k) number K964111. The device is classified under product code KQT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LITHOVAC SUCTION/ASPIRATION PROBE?

LITHOVAC SUCTION/ASPIRATION PROBE is a medical device that received FDA 510(k) clearance on 1996-12-16. The listed applicant is Electro Medical Systems SA. The 510(k) number is K964111.

When did LITHOVAC SUCTION/ASPIRATION PROBE receive FDA 510(k) clearance?

LITHOVAC SUCTION/ASPIRATION PROBE received FDA 510(k) clearance on 1996-12-16, under 510(k) number K964111.

Who is the listed applicant for LITHOVAC SUCTION/ASPIRATION PROBE?

The FDA 510(k) record lists Electro Medical Systems SA as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LITHOVAC SUCTION/ASPIRATION PROBE?

The FDA product code for LITHOVAC SUCTION/ASPIRATION PROBE is KQT.

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 Electro Medical Systems SA 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.

K022328EMS PIEZON MASTER 600K022119EMS AIR-FLOW HANDY 2 DENTAL HANDPIECEK012445EMS SWISS LITHOCLAST MASTER (A.K.A. SWISS LITHOCLAST ULTRA)K002484EMS SWISS ORTHOCLAST CHISELS FOR NON-CEMENTED PROSTHESIS REMOVALK992251SWISS LITHOCLAST MULTIPURPOSE PROBEK963285EMS SWISS LITHOCLAST LITHOTRIPTER

View all 9 devices →

Related Devices (Code: KQT)

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.

K921451EVACUATOR, GASTRO-UROLOGYNorthgate Technologies, Inc.K921088EVACUATOR, GASTRO-UROLOGYNorthgate Technologies, Inc.K910728CLEANFLOW SYSTEMMitron Technologies, Inc.K880099VAN-TEC BLADDER EVACUATORVan-Tec, Inc.K874493BELLA - VAC IRRIGATORBel-Can IndustriesK860266ELLIK EVACUATORR. J. Ltd., Ind.

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.

↑