16ch T/R Hand Wrist Coil
K-Number: K162623 · 2016-12-09
Device Summary
Frequently Asked Questions
What is the 16ch T/R Hand Wrist Coil?
16ch T/R Hand Wrist Coil is a medical device that received FDA 510(k) clearance on 2016-12-09. The listed applicant is Quality Electrodynamics, LLC. The 510(k) number is K162623.
When did 16ch T/R Hand Wrist Coil receive FDA 510(k) clearance?
16ch T/R Hand Wrist Coil received FDA 510(k) clearance on 2016-12-09, under 510(k) number K162623.
Who is the listed applicant for 16ch T/R Hand Wrist Coil?
The FDA 510(k) record lists Quality Electrodynamics, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 16ch T/R Hand Wrist Coil?
The FDA product code for 16ch T/R Hand Wrist Coil 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 Quality Electrodynamics, LLC 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.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.