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)

SHINMED MODE SW-988 UNTRASONIC NEBULIZER

K-Number: K031370 · 2004-09-01

Decision Date2004-09-01
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SHINMED MODE SW-988 UNTRASONIC NEBULIZER is the device name listed in this FDA 510(k) record. The listed applicant is Shining World Health Care Co., Ltd.. It received FDA 510(k) clearance on 2004-09-01 under 510(k) number K031370. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SHINMED MODE SW-988 UNTRASONIC NEBULIZER?

SHINMED MODE SW-988 UNTRASONIC NEBULIZER is a medical device that received FDA 510(k) clearance on 2004-09-01. The listed applicant is Shining World Health Care Co., Ltd.. The 510(k) number is K031370.

When did SHINMED MODE SW-988 UNTRASONIC NEBULIZER receive FDA 510(k) clearance?

SHINMED MODE SW-988 UNTRASONIC NEBULIZER received FDA 510(k) clearance on 2004-09-01, under 510(k) number K031370.

Who is the listed applicant for SHINMED MODE SW-988 UNTRASONIC NEBULIZER?

The FDA 510(k) record lists Shining World Health Care Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SHINMED MODE SW-988 UNTRASONIC NEBULIZER?

The FDA product code for SHINMED MODE SW-988 UNTRASONIC NEBULIZER is CAF.

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 Shining World Health Care 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.

Related Devices (Code: CAF)

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.

↑