FDA 510(k)

ARTHROSCOPE FOR SMALL JOINT AFTER FELDKAMP, MODEL 8871.011

K-Number: K940179 · 1995-05-23

ApplicantRichard Wolf Medical Instruments Corp.

Decision Date1995-05-23

Product CodeHRX

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

ARTHROSCOPE FOR SMALL JOINT AFTER FELDKAMP, MODEL 8871.011 is the device name listed in this FDA 510(k) record. The listed applicant is Richard Wolf Medical Instruments Corp.. It received FDA 510(k) clearance on 1995-05-23 under 510(k) number K940179. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTHROSCOPE FOR SMALL JOINT AFTER FELDKAMP, MODEL 8871.011?

ARTHROSCOPE FOR SMALL JOINT AFTER FELDKAMP, MODEL 8871.011 is a medical device that received FDA 510(k) clearance on 1995-05-23. The listed applicant is Richard Wolf Medical Instruments Corp.. The 510(k) number is K940179.

When did ARTHROSCOPE FOR SMALL JOINT AFTER FELDKAMP, MODEL 8871.011 receive FDA 510(k) clearance?

ARTHROSCOPE FOR SMALL JOINT AFTER FELDKAMP, MODEL 8871.011 received FDA 510(k) clearance on 1995-05-23, under 510(k) number K940179.

Who is the listed applicant for ARTHROSCOPE FOR SMALL JOINT AFTER FELDKAMP, MODEL 8871.011?

The FDA 510(k) record lists Richard Wolf Medical Instruments Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ARTHROSCOPE FOR SMALL JOINT AFTER FELDKAMP, MODEL 8871.011?

The FDA product code for ARTHROSCOPE FOR SMALL JOINT AFTER FELDKAMP, MODEL 8871.011 is HRX.

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_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Richard Wolf Medical Instruments Corp. as applicant

K151282core nova Complete Operating Room Endoscopy K130423THE RICHARD WOLF ENDOCAM LOGIC HD CAMERA SYSTEM 5525 K121724ENDOLIGHT LED 1.1 ENDOLIGHTLED 1.2 K120898KEYPORT SYSTEM, INCLUDES: KEYPORT SILICONE SEALING INSERT 8850XXX KEYPORT TRUCAR 8850XX KEYPORT TROCAR 8850XX SEALING CA K090776MEGAPULSE LASER SYSTEM AND FIBERS K080617POWER DRIVE ART1 2304 WITH MOTOR HANDLES, TOOLS AND ACCESSORIES

View all 142 devices →

Related Devices (Code: HRX)

K260203Fule Vertebroplasty Balloon CatheterBeijing Fule Science & Technology Development Co., Ltd.K254103HOPKINS Telescopes for ArthroscopyKarl Storz SE & CO. KG K252790Digital ClarusScope System and Digital NeuroPEN SystemClarus Medical, LLC K253523Freedom DS™ Decompression SystemSpinal Simplicity K252546VantageTM Lumbar Decompression KitAllevion Medical, LLC K253217MiiS Horus Arthroscope (EJA 100); MiiS Horus Endoscope Display System -Tablet (EDS 500); MiiS Horus Endoscope Display System -Video Box (EVS 700)Medimaging Integrated Solution, Inc (Miis)

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.