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FDA 510(k)

MICROSCIS(TM) INTROCULAR SCISSOR SYSTEM

K-Number: K913837 · 1991-11-05

ApplicantVision Medical, Inc.
Decision Date1991-11-05
Product CodeHQE
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MICROSCIS(TM) INTROCULAR SCISSOR SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Vision Medical, Inc.. It received FDA 510(k) clearance on 1991-11-05 under 510(k) number K913837. The device is classified under product code HQE. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROSCIS(TM) INTROCULAR SCISSOR SYSTEM?

MICROSCIS(TM) INTROCULAR SCISSOR SYSTEM is a medical device that received FDA 510(k) clearance on 1991-11-05. The listed applicant is Vision Medical, Inc.. The 510(k) number is K913837.

When did MICROSCIS(TM) INTROCULAR SCISSOR SYSTEM receive FDA 510(k) clearance?

MICROSCIS(TM) INTROCULAR SCISSOR SYSTEM received FDA 510(k) clearance on 1991-11-05, under 510(k) number K913837.

Who is the listed applicant for MICROSCIS(TM) INTROCULAR SCISSOR SYSTEM?

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

What is the FDA product code for MICROSCIS(TM) INTROCULAR SCISSOR SYSTEM?

The FDA product code for MICROSCIS(TM) INTROCULAR SCISSOR SYSTEM is HQE.

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 Vision 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.

K913273DROLITE(TM) LIGHT SOURCE

Related Devices (Code: HQE)

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.

K212763UniVit HE, UniVit UHSVisioncare Devices, LLCK170183Cetus system, Cetus probeA.R.C Laser GmbHK153168Bi-Blade Vitrectomy CutterMedical Instrument Development LaboratoriesK121675VERSAVITSynergetics, Inc.K120170PROCARE PLUS VITRECTOMY SYSTEMVisioncare Devices, Inc.K102222ULTIMATE VIT ENHAMCER (UVE)Medical Instrument Development Laboratories, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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