Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

EMG SUCTION UNIT

K-Number: K112421 · 2011-09-01

Decision Date2011-09-01
Product CodeJCX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

EMG SUCTION UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Emg Technology Co., Ltd.. It received FDA 510(k) clearance on 2011-09-01 under 510(k) number K112421. The device is classified under product code JCX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EMG SUCTION UNIT?

EMG SUCTION UNIT is a medical device that received FDA 510(k) clearance on 2011-09-01. The listed applicant is Emg Technology Co., Ltd.. The 510(k) number is K112421.

When did EMG SUCTION UNIT receive FDA 510(k) clearance?

EMG SUCTION UNIT received FDA 510(k) clearance on 2011-09-01, under 510(k) number K112421.

Who is the listed applicant for EMG SUCTION UNIT?

The FDA 510(k) record lists Emg Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EMG SUCTION UNIT?

The FDA product code for EMG SUCTION UNIT is JCX.

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 Emg Technology 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 11 devices →

Related Devices (Code: JCX)

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.

↑