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FDA 510(k)

MODEL 700GE1500 CARDIAC VASCULAR COIL FOR G.E. 1.5T SIGNA

K-Number: K933295 · 1994-03-17

ApplicantMedic, Inc.
Decision Date1994-03-17
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MODEL 700GE1500 CARDIAC VASCULAR COIL FOR G.E. 1.5T SIGNA is the device name listed in this FDA 510(k) record. The listed applicant is Medic, Inc.. It received FDA 510(k) clearance on 1994-03-17 under 510(k) number K933295. 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 700GE1500 CARDIAC VASCULAR COIL FOR G.E. 1.5T SIGNA?

MODEL 700GE1500 CARDIAC VASCULAR COIL FOR G.E. 1.5T SIGNA is a medical device that received FDA 510(k) clearance on 1994-03-17. The listed applicant is Medic, Inc.. The 510(k) number is K933295.

When did MODEL 700GE1500 CARDIAC VASCULAR COIL FOR G.E. 1.5T SIGNA receive FDA 510(k) clearance?

MODEL 700GE1500 CARDIAC VASCULAR COIL FOR G.E. 1.5T SIGNA received FDA 510(k) clearance on 1994-03-17, under 510(k) number K933295.

Who is the listed applicant for MODEL 700GE1500 CARDIAC VASCULAR COIL FOR G.E. 1.5T SIGNA?

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 700GE1500 CARDIAC VASCULAR COIL FOR G.E. 1.5T SIGNA?

The FDA product code for MODEL 700GE1500 CARDIAC VASCULAR COIL FOR G.E. 1.5T SIGNA is LNH.

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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 COILK942873MODEL #700TO3500 NECK/ABDOMINAL COILK942875MODEL #900TO3500 HEAD/NECK COILK942355MODEL #310T03500 WRIST COIL

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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.

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