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)

D7113 ANVIL CUTTER AND D7112 AIR-POWERED HANDLE

K-Number: K915745 · 1992-03-13

ApplicantStorz Instrument Co.
Decision Date1992-03-13
Product CodeHQE
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

D7113 ANVIL CUTTER AND D7112 AIR-POWERED HANDLE is the device name listed in this FDA 510(k) record. The listed applicant is Storz Instrument Co.. It received FDA 510(k) clearance on 1992-03-13 under 510(k) number K915745. 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 D7113 ANVIL CUTTER AND D7112 AIR-POWERED HANDLE?

D7113 ANVIL CUTTER AND D7112 AIR-POWERED HANDLE is a medical device that received FDA 510(k) clearance on 1992-03-13. The listed applicant is Storz Instrument Co.. The 510(k) number is K915745.

When did D7113 ANVIL CUTTER AND D7112 AIR-POWERED HANDLE receive FDA 510(k) clearance?

D7113 ANVIL CUTTER AND D7112 AIR-POWERED HANDLE received FDA 510(k) clearance on 1992-03-13, under 510(k) number K915745.

Who is the listed applicant for D7113 ANVIL CUTTER AND D7112 AIR-POWERED HANDLE?

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

What is the FDA product code for D7113 ANVIL CUTTER AND D7112 AIR-POWERED HANDLE?

The FDA product code for D7113 ANVIL CUTTER AND D7112 AIR-POWERED HANDLE 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 Storz Instrument 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.

K980100STORZ DP4210 VENTURI ECONOMY ANTERIOR PACK AND DP5000 ASC DAYPACKK980488STORZ MILLENNIUM MICROSURGICL SYSTEM HIGH SPEED VITRECTOMY SYSTEMK972664STORZ MILLENNIUM VISCOUS FLUID SYSTEMK971439STORZ MICROFLOW AND STORZ STANDARD PHACOEMULSIFICATION NEEDLESK964743STORZ E8010 ERGOTEC/PREMIERE ADAPTORK960024STORZ D7120 PHACO HANDPIECE MAINTENANCE KIT & STORZ D7125 PHACO HANDPIECE NEEDLE WRENCH

View all 101 devices →

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

View on FDA Database →

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

↑