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)

MODEL #100GE1500 LOWER EXTREM QUAD DETECT ARRAY COIL

K-Number: K933659 · 1993-11-22

ApplicantMedic, Inc.
Decision Date1993-11-22
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MODEL #100GE1500 LOWER EXTREM QUAD DETECT ARRAY COIL is the device name listed in this FDA 510(k) record. The listed applicant is Medic, Inc.. It received FDA 510(k) clearance on 1993-11-22 under 510(k) number K933659. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL #100GE1500 LOWER EXTREM QUAD DETECT ARRAY COIL?

MODEL #100GE1500 LOWER EXTREM QUAD DETECT ARRAY COIL is a medical device that received FDA 510(k) clearance on 1993-11-22. The listed applicant is Medic, Inc.. The 510(k) number is K933659.

When did MODEL #100GE1500 LOWER EXTREM QUAD DETECT ARRAY COIL receive FDA 510(k) clearance?

MODEL #100GE1500 LOWER EXTREM QUAD DETECT ARRAY COIL received FDA 510(k) clearance on 1993-11-22, under 510(k) number K933659.

Who is the listed applicant for MODEL #100GE1500 LOWER EXTREM QUAD DETECT ARRAY COIL?

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

What is the FDA product code for MODEL #100GE1500 LOWER EXTREM QUAD DETECT ARRAY COIL?

The FDA product code for MODEL #100GE1500 LOWER EXTREM QUAD DETECT ARRAY COIL is LNH.

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 Medic, 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.

K0223951.5T SCANMED PV ARRAYK951649MODEL #801GE1500 PEDIATRIC ARRAY COILK942874MODEL #300TO3500 SHOULDER COILK942875MODEL #900TO3500 HEAD/NECK COILK942873MODEL #700TO3500 NECK/ABDOMINAL COILK942355MODEL #310T03500 WRIST COIL

View all 12 devices →

Related Devices (Code: LNH)

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.

K261758Embrace Vision Neonatal MRI SystemAspect Imaging, Ltd.K261283APERTO Lucent MRI SystemFujifilm CorporationK260758MAGNETOM Free.Max; MAGNETOM Free.StarSiemens Shenzhen Magnetic Resonance , Ltd.K262622Swoop® Portable MR Imaging® SystemHyperfine, Inc.K254250MagicScan-1.5, GreenMR Serenity 1.5TXingaoyi Medical Equipment Co.,LtdK253808AIR Recon DLGE Medical Systems

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.

↑