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FDA 510(k)

JIAJIAN CMN STIMULATOR

K-Number: K130768 · 2013-08-16

Decision Date2013-08-16
Product CodeBWK
DecisionSubstantially Equivalent

Device Summary

JIAJIAN CMN STIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Wuxi Jiajian Medical Instrument Co., Ltd.. It received FDA 510(k) clearance on 2013-08-16 under 510(k) number K130768. The device is classified under product code BWK. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JIAJIAN CMN STIMULATOR?

JIAJIAN CMN STIMULATOR is a medical device that received FDA 510(k) clearance on 2013-08-16. The listed applicant is Wuxi Jiajian Medical Instrument Co., Ltd.. The 510(k) number is K130768.

When did JIAJIAN CMN STIMULATOR receive FDA 510(k) clearance?

JIAJIAN CMN STIMULATOR received FDA 510(k) clearance on 2013-08-16, under 510(k) number K130768.

Who is the listed applicant for JIAJIAN CMN STIMULATOR?

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

What is the FDA product code for JIAJIAN CMN STIMULATOR?

The FDA product code for JIAJIAN CMN STIMULATOR is BWK.

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 Wuxi Jiajian Medical Instrument Co., Ltd. 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 12 devices →

Related Devices (Code: BWK)

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.

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