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FDA 510(k)

MODEL #QWH-63, QUADRATURE WRIST AND HAND COIL

K-Number: K931008 · 1993-06-18

ApplicantMri Devices Corp.
Decision Date1993-06-18
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MODEL #QWH-63, QUADRATURE WRIST AND HAND COIL 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 1993-06-18 under 510(k) number K931008. 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 #QWH-63, QUADRATURE WRIST AND HAND COIL?

MODEL #QWH-63, QUADRATURE WRIST AND HAND COIL is a medical device that received FDA 510(k) clearance on 1993-06-18. The listed applicant is Mri Devices Corp.. The 510(k) number is K931008.

When did MODEL #QWH-63, QUADRATURE WRIST AND HAND COIL receive FDA 510(k) clearance?

MODEL #QWH-63, QUADRATURE WRIST AND HAND COIL received FDA 510(k) clearance on 1993-06-18, under 510(k) number K931008.

Who is the listed applicant for MODEL #QWH-63, QUADRATURE WRIST AND HAND COIL?

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 #QWH-63, QUADRATURE WRIST AND HAND COIL?

The FDA product code for MODEL #QWH-63, QUADRATURE WRIST AND HAND COIL 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)

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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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