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)

IMPLANTABLE PULSE GENERATORS

K-Number: K925106 · 1993-10-06

ApplicantMedtronic Vascular
Decision Date1993-10-06
Product CodeDYX
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

IMPLANTABLE PULSE GENERATORS is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 1993-10-06 under 510(k) number K925106. The device is classified under product code DYX. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMPLANTABLE PULSE GENERATORS?

IMPLANTABLE PULSE GENERATORS is a medical device that received FDA 510(k) clearance on 1993-10-06. The listed applicant is Medtronic Vascular. The 510(k) number is K925106.

When did IMPLANTABLE PULSE GENERATORS receive FDA 510(k) clearance?

IMPLANTABLE PULSE GENERATORS received FDA 510(k) clearance on 1993-10-06, under 510(k) number K925106.

Who is the listed applicant for IMPLANTABLE PULSE GENERATORS?

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

What is the FDA product code for IMPLANTABLE PULSE GENERATORS?

The FDA product code for IMPLANTABLE PULSE GENERATORS is DYX.

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 Medtronic Vascular 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.

K232570Steerant™ Super Stiff GuidewireK2321906F Sherpa NX Balanced Guide Catheter, 7F Sherpa NX Balanced Guide CatheterK2301565F Launcher Guide Catheter, 6F Launcher Guide Catheter, 7F Launcher Guide Catheter, 8F Launcher Guide CatheterK220773Everest 20 Inflation Device and 3-way Stopcock (AC2200);Everest 30 Inflation Device and 3-way Stopcock (AC3200);Everest 20 Survival Kit containing:1. Everest 20 Device with 3-way Stopcock, 2. Piton Y-Adaptor ,3. Metal Guidewire Insertion Needle, 4. Torque Handle (AC2205P); Everest 30 Survival Kit containing:1. Everest 30 Device with 3-way Stopcock, 2. Piton Y-Adaptor,3. Metal Guidewire Insertion Needle, 4. Torque Handle (AC3205P)K192296Medtronic 6F Taiga Guiding CatheterK173515Admiral Xtreme

View all 474 devices →

Related Devices (Code: DYX)

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.

K162046MINNE TIES MMF Suture SystemSummit Medical, Inc.K061271ERCH ARCH BAR, MODEL 38-690-00KLS-Martin L.P.K031207SAFETY RELEASE ARCH BAR KITCasey Surgical, LLCK030605RAPID IMFZygomatics , Ltd.K990212LOCKJAW 15 MINUTE INTERMAXILLARY FIXATION SYSTEM,MODEL LJ100-00Doctor'S Research Group, Inc.K991004SYNTHES QUICK LOCK IMF SYSTEMSynthes (Usa)

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.

↑