FDA 510(k)

Multi-parameter detector

K-Number: K231116 · 2024-06-15

ApplicantZhongshan Jinli Electronic Weighing Equipment Co., Ltd.

Decision Date2024-06-15

Product CodeMNW

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

Multi-parameter detector is the device name listed in this FDA 510(k) record. The listed applicant is Zhongshan Jinli Electronic Weighing Equipment Co., Ltd.. It received FDA 510(k) clearance on 2024-06-15 under 510(k) number K231116. The device is classified under product code MNW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Multi-parameter detector?

Multi-parameter detector is a medical device that received FDA 510(k) clearance on 2024-06-15. The listed applicant is Zhongshan Jinli Electronic Weighing Equipment Co., Ltd.. The 510(k) number is K231116.

When did Multi-parameter detector receive FDA 510(k) clearance?

Multi-parameter detector received FDA 510(k) clearance on 2024-06-15, under 510(k) number K231116.

Who is the listed applicant for Multi-parameter detector?

The FDA 510(k) record lists Zhongshan Jinli Electronic Weighing Equipment Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Multi-parameter detector?

The FDA product code for Multi-parameter detector is MNW.

Other records listing Zhongshan Jinli Electronic Weighing Equipment 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.

K201582Non-contact Electronic Forehead Infrared Thermometer

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.