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FDA 510(k)

MODEL #801GE1500 PEDIATRIC ARRAY COIL

K-Number: K951649 · 1995-06-22

ApplicantMedic, Inc.
Decision Date1995-06-22
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MODEL #801GE1500 PEDIATRIC 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 1995-06-22 under 510(k) number K951649. 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 #801GE1500 PEDIATRIC ARRAY COIL?

MODEL #801GE1500 PEDIATRIC ARRAY COIL is a medical device that received FDA 510(k) clearance on 1995-06-22. The listed applicant is Medic, Inc.. The 510(k) number is K951649.

When did MODEL #801GE1500 PEDIATRIC ARRAY COIL receive FDA 510(k) clearance?

MODEL #801GE1500 PEDIATRIC ARRAY COIL received FDA 510(k) clearance on 1995-06-22, under 510(k) number K951649.

Who is the listed applicant for MODEL #801GE1500 PEDIATRIC 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 #801GE1500 PEDIATRIC ARRAY COIL?

The FDA product code for MODEL #801GE1500 PEDIATRIC 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.

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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 ARRAYK942874MODEL #300TO3500 SHOULDER COILK942873MODEL #700TO3500 NECK/ABDOMINAL COILK942875MODEL #900TO3500 HEAD/NECK COILK942355MODEL #310T03500 WRIST COILK940874MODEL 900GE1500 HEAD/NECK 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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