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)

OCULAR PRESSURE REDUCER (MCCANNEL)

K-Number: K852032 · 1985-08-12

ApplicantVisitec Co.
Decision Date1985-08-12
Product CodeLCC
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

OCULAR PRESSURE REDUCER (MCCANNEL) is the device name listed in this FDA 510(k) record. The listed applicant is Visitec Co.. It received FDA 510(k) clearance on 1985-08-12 under 510(k) number K852032. The device is classified under product code LCC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OCULAR PRESSURE REDUCER (MCCANNEL)?

OCULAR PRESSURE REDUCER (MCCANNEL) is a medical device that received FDA 510(k) clearance on 1985-08-12. The listed applicant is Visitec Co.. The 510(k) number is K852032.

When did OCULAR PRESSURE REDUCER (MCCANNEL) receive FDA 510(k) clearance?

OCULAR PRESSURE REDUCER (MCCANNEL) received FDA 510(k) clearance on 1985-08-12, under 510(k) number K852032.

Who is the listed applicant for OCULAR PRESSURE REDUCER (MCCANNEL)?

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

What is the FDA product code for OCULAR PRESSURE REDUCER (MCCANNEL)?

The FDA product code for OCULAR PRESSURE REDUCER (MCCANNEL) is LCC.

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 Visitec Co. 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.

K953394VISITEC COLLAR BUTTON CATHETER {GRIFFITHS}K945114VISITEC SCLERAL PLUGK945738VISIFLEX OPHTHALMIC SURGICAL INCISE DRAPEK945172VISITEC SILICONE RETINAL IMPLANTS/EXPLANTSK942234VISITEC PRECISE-POINTK934269FIBEROPTIC ILLUMINATED INSTRUMENTS

View all 49 devices →

Related Devices (Code: LCC)

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.

K112952ILWAIT TIMER OCULOPRESSOROryx Medical Pty, Ltd.K946194WEE BAG O'MERCURYMicrosurgical Technology, Inc.K840004WEE BAG O'MERCURYSurgi-Quip Inc.UK820526RELIEF VALVE-HONAN INTRAOC. PRESSUREThe Lebanon Corp.K792255NEVYAS AUTOPRESS EYE COMPRESSORKeeler Optical Products , Ltd.

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.

↑