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)

CARE SU01A SUCTION ASPIRATOR

K-Number: K130001 · 2013-07-25

Decision Date2013-07-25
Product CodeJCX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CARE SU01A SUCTION ASPIRATOR is the device name listed in this FDA 510(k) record. The listed applicant is Foshan Care Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2013-07-25 under 510(k) number K130001. 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 CARE SU01A SUCTION ASPIRATOR?

CARE SU01A SUCTION ASPIRATOR is a medical device that received FDA 510(k) clearance on 2013-07-25. The listed applicant is Foshan Care Medical Technology Co., Ltd.. The 510(k) number is K130001.

When did CARE SU01A SUCTION ASPIRATOR receive FDA 510(k) clearance?

CARE SU01A SUCTION ASPIRATOR received FDA 510(k) clearance on 2013-07-25, under 510(k) number K130001.

Who is the listed applicant for CARE SU01A SUCTION ASPIRATOR?

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

What is the FDA product code for CARE SU01A SUCTION ASPIRATOR?

The FDA product code for CARE SU01A SUCTION ASPIRATOR 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 Foshan Care Medical 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.

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.

↑