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)

SOLOS EYESITE CANNULAS

K-Number: K872610 · 1987-07-31

ApplicantSolos Ophthalmology
Decision Date1987-07-31
Product CodeHMX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SOLOS EYESITE CANNULAS is the device name listed in this FDA 510(k) record. The listed applicant is Solos Ophthalmology. It received FDA 510(k) clearance on 1987-07-31 under 510(k) number K872610. The device is classified under product code HMX. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SOLOS EYESITE CANNULAS?

SOLOS EYESITE CANNULAS is a medical device that received FDA 510(k) clearance on 1987-07-31. The listed applicant is Solos Ophthalmology. The 510(k) number is K872610.

When did SOLOS EYESITE CANNULAS receive FDA 510(k) clearance?

SOLOS EYESITE CANNULAS received FDA 510(k) clearance on 1987-07-31, under 510(k) number K872610.

Who is the listed applicant for SOLOS EYESITE CANNULAS?

The FDA 510(k) record lists Solos Ophthalmology as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SOLOS EYESITE CANNULAS?

The FDA product code for SOLOS EYESITE CANNULAS is HMX.

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 Solos Ophthalmology 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.

K874334SOLOS SINGLE USE TITANIUM TIPK872611SOLOS EYESITE CAP SLEEVEK872612SOLOS EYESITE SPONGESK872620SOLOS EYESITE DRAPES

Related Devices (Code: HMX)

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.

K010305WEISS RETINAL CANNULAMicron Surgical, Inc.K000457VERTEFUSION-PHOTODYNAMIC THERAPY PAK, MODEL 11000 SERIES; PHOTOFUSION-PHOTODYNAMIC THERAPY PAK, MODEL 12000 SERIESRetinalabs.ComK970873ENDOSOFT SOFT TIP NEEDLE (20 GA. AND 19 GA.)American Medical Devices, Inc.K943932STERISEAL OPHTHALMIC CANNULAPharma-Plast, Ltd.K942403INFUSION CANNULAMicrosurgical Technology, Inc.K934844INTER TIP TMicrosurgical Technology, 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.

↑