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

FDA 510(k)

Single Use Aspiration Needle NA-U201H

K-Number: K181994 · 2018-10-31

Decision Date2018-10-31
Product CodeFCG
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Single Use Aspiration Needle NA-U201H is a medical device manufactured by Olympus Medical Systems Corp.. It received FDA 510(k) clearance on 2018-10-31 under approval number K181994. The device is classified under product code FCG. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Single Use Aspiration Needle NA-U201H?

Single Use Aspiration Needle NA-U201H is a medical device that received FDA 510(k) clearance on 2018-10-31. It is manufactured by Olympus Medical Systems Corp.. The 510(k) number is K181994.

When was Single Use Aspiration Needle NA-U201H approved by the FDA?

Single Use Aspiration Needle NA-U201H received FDA 510(k) clearance on 2018-10-31, under approval number K181994.

What company makes Single Use Aspiration Needle NA-U201H?

Single Use Aspiration Needle NA-U201H is manufactured by Olympus Medical Systems Corp..

What is the FDA product code for Single Use Aspiration Needle NA-U201H?

The FDA product code for Single Use Aspiration Needle NA-U201H is FCG.

Related Clinical Trials

Related PubMed Literature

Other Devices by Olympus Medical Systems Corp.

View all 77 devices →

Related Devices (Code: FCG)

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.