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FDA 510(k)

HRW-42 WRIST ARRAY COIL FOR 1.0 TESLA

K-Number: K001713 · 2000-06-14

Decision Date2000-06-14
Product CodeMOS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

HRW-42 WRIST ARRAY COIL FOR 1.0 TESLA 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 2000-06-14 under 510(k) number K001713. The device is classified under product code MOS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HRW-42 WRIST ARRAY COIL FOR 1.0 TESLA?

HRW-42 WRIST ARRAY COIL FOR 1.0 TESLA is a medical device that received FDA 510(k) clearance on 2000-06-14. The listed applicant is Mri Devices Corp.. The 510(k) number is K001713.

When did HRW-42 WRIST ARRAY COIL FOR 1.0 TESLA receive FDA 510(k) clearance?

HRW-42 WRIST ARRAY COIL FOR 1.0 TESLA received FDA 510(k) clearance on 2000-06-14, under 510(k) number K001713.

Who is the listed applicant for HRW-42 WRIST ARRAY COIL FOR 1.0 TESLA?

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 HRW-42 WRIST ARRAY COIL FOR 1.0 TESLA?

The FDA product code for HRW-42 WRIST ARRAY COIL FOR 1.0 TESLA is MOS.

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.

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.

View all 71 devices →

Related Devices (Code: MOS)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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