FDA 510(k)

MODEL CG-WHC18-H150-AP - WRIST HAND COIL 1.5T 4 CH,

K-Number: K071882 · 2007-07-18

ApplicantShanghai Chenguang Medical Technologies Co, Ltd.

Decision Date2007-07-18

Product CodeMOS

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

MODEL CG-WHC18-H150-AP - WRIST HAND COIL 1.5T 4 CH, is the device name listed in this FDA 510(k) record. The listed applicant is Shanghai Chenguang Medical Technologies Co, Ltd.. It received FDA 510(k) clearance on 2007-07-18 under 510(k) number K071882. 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 MODEL CG-WHC18-H150-AP - WRIST HAND COIL 1.5T 4 CH,?

MODEL CG-WHC18-H150-AP - WRIST HAND COIL 1.5T 4 CH, is a medical device that received FDA 510(k) clearance on 2007-07-18. The listed applicant is Shanghai Chenguang Medical Technologies Co, Ltd.. The 510(k) number is K071882.

When did MODEL CG-WHC18-H150-AP - WRIST HAND COIL 1.5T 4 CH, receive FDA 510(k) clearance?

MODEL CG-WHC18-H150-AP - WRIST HAND COIL 1.5T 4 CH, received FDA 510(k) clearance on 2007-07-18, under 510(k) number K071882.

Who is the listed applicant for MODEL CG-WHC18-H150-AP - WRIST HAND COIL 1.5T 4 CH,?

The FDA 510(k) record lists Shanghai Chenguang Medical Technologies Co, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODEL CG-WHC18-H150-AP - WRIST HAND COIL 1.5T 4 CH,?

The FDA product code for MODEL CG-WHC18-H150-AP - WRIST HAND COIL 1.5T 4 CH, is MOS.

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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.