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)

REPROCESSED PHACOEMUISIFICATION TIPS

K-Number: K050518 · 2005-09-23

ApplicantAlliance Medical, Inc.
Decision Date2005-09-23
Product CodeNKX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

REPROCESSED PHACOEMUISIFICATION TIPS is the device name listed in this FDA 510(k) record. The listed applicant is Alliance Medical, Inc.. It received FDA 510(k) clearance on 2005-09-23 under 510(k) number K050518. The device is classified under product code NKX. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REPROCESSED PHACOEMUISIFICATION TIPS?

REPROCESSED PHACOEMUISIFICATION TIPS is a medical device that received FDA 510(k) clearance on 2005-09-23. The listed applicant is Alliance Medical, Inc.. The 510(k) number is K050518.

When did REPROCESSED PHACOEMUISIFICATION TIPS receive FDA 510(k) clearance?

REPROCESSED PHACOEMUISIFICATION TIPS received FDA 510(k) clearance on 2005-09-23, under 510(k) number K050518.

Who is the listed applicant for REPROCESSED PHACOEMUISIFICATION TIPS?

The FDA 510(k) record lists Alliance Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for REPROCESSED PHACOEMUISIFICATION TIPS?

The FDA product code for REPROCESSED PHACOEMUISIFICATION TIPS is NKX.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Alliance Medical, Inc. 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.

K051438VANGUARD REPROCESSED COMPRESSION GARMENTS (HILL-ROM)K030187REPROCESSED ELECTROPHYSIOLOGY CATHETERK021654REPROCESSED COMPRESSION SLEEVEK012634REPROCESSED EXTERNAL FIXATION DEVICEK012630REPROCESSED LINVATEC ARTHROSCOPIC BURSK012613REPROCSSED LINVATEC SHAVERS

View all 11 devices →

Related Devices (Code: NKX)

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.

K060648REPROCESSED PHACOEMULSIFICATION TIPSAlliance Medical Corp.K030179MEDISISS PHACOEMULSIFICATION TIPS/NEEDLESSurgical Instruments Service and Savings, Inc.K012698VANGUARD REPROCESSED PHACOEMULSIFICATIONVanguard Medical Concepts, Inc.K012579REPROCESSED PHACO TIPSSterilmed, Inc.

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.

↑