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FDA 510(k)

MODEL #QSC-200-4C AND QSC-165-4C ARRAY SHOULDER COILS

K-Number: K961366 · 1996-07-03

ApplicantMri Devices Corp.
Decision Date1996-07-03
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MODEL #QSC-200-4C AND QSC-165-4C ARRAY SHOULDER COILS is the device name listed in this FDA 510(k) record. The listed applicant is Mri Devices Corp.. It received FDA 510(k) clearance on 1996-07-03 under 510(k) number K961366. 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 #QSC-200-4C AND QSC-165-4C ARRAY SHOULDER COILS?

MODEL #QSC-200-4C AND QSC-165-4C ARRAY SHOULDER COILS is a medical device that received FDA 510(k) clearance on 1996-07-03. The listed applicant is Mri Devices Corp.. The 510(k) number is K961366.

When did MODEL #QSC-200-4C AND QSC-165-4C ARRAY SHOULDER COILS receive FDA 510(k) clearance?

MODEL #QSC-200-4C AND QSC-165-4C ARRAY SHOULDER COILS received FDA 510(k) clearance on 1996-07-03, under 510(k) number K961366.

Who is the listed applicant for MODEL #QSC-200-4C AND QSC-165-4C ARRAY SHOULDER COILS?

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

What is the FDA product code for MODEL #QSC-200-4C AND QSC-165-4C ARRAY SHOULDER COILS?

The FDA product code for MODEL #QSC-200-4C AND QSC-165-4C ARRAY SHOULDER COILS is LNH.

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Other records listing Mri Devices Corp. 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.

K041286DYNACAD V1.0K041481MODEL BBC-127 BIOPSY BREAST COILK040348MODIFICATION TO HNC-127-INT NEUROVASCULAR ARRAY COILK040349MODIFICATION TO HRW-127 WRIST ARRAY COILK040288QSC-127-INT SHOULDER ARRAY COIL SETK033447CLIPLOC SOFT TISSUE MARKER 18G/100MM (4), /130MM (5 1/8), /150MM (6), MODELS 12370, 12372, 12376

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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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