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FDA 510(k)

MODEL #SCT-32 AUTO QUADRATURE SPINE COIL TRANSPORT

K-Number: K913441 · 1991-10-21

ApplicantMri Devices Corp.
Decision Date1991-10-21
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MODEL #SCT-32 AUTO QUADRATURE SPINE COIL TRANSPORT 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 1991-10-21 under 510(k) number K913441. 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 #SCT-32 AUTO QUADRATURE SPINE COIL TRANSPORT?

MODEL #SCT-32 AUTO QUADRATURE SPINE COIL TRANSPORT is a medical device that received FDA 510(k) clearance on 1991-10-21. The listed applicant is Mri Devices Corp.. The 510(k) number is K913441.

When did MODEL #SCT-32 AUTO QUADRATURE SPINE COIL TRANSPORT receive FDA 510(k) clearance?

MODEL #SCT-32 AUTO QUADRATURE SPINE COIL TRANSPORT received FDA 510(k) clearance on 1991-10-21, under 510(k) number K913441.

Who is the listed applicant for MODEL #SCT-32 AUTO QUADRATURE SPINE COIL TRANSPORT?

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 #SCT-32 AUTO QUADRATURE SPINE COIL TRANSPORT?

The FDA product code for MODEL #SCT-32 AUTO QUADRATURE SPINE COIL TRANSPORT 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 COILK040349MODIFICATION TO HRW-127 WRIST ARRAY COILK040348MODIFICATION TO HNC-127-INT NEUROVASCULAR 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.

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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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