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FDA 510(k)

KSEA C-MOUNT ARTHROSCOPES

K-Number: K983142 · 1998-12-07

ApplicantKarl Storz Endoscopy
Decision Date1998-12-07
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

KSEA C-MOUNT ARTHROSCOPES is the device name listed in this FDA 510(k) record. The listed applicant is Karl Storz Endoscopy. It received FDA 510(k) clearance on 1998-12-07 under 510(k) number K983142. 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 KSEA C-MOUNT ARTHROSCOPES?

KSEA C-MOUNT ARTHROSCOPES is a medical device that received FDA 510(k) clearance on 1998-12-07. The listed applicant is Karl Storz Endoscopy. The 510(k) number is K983142.

When did KSEA C-MOUNT ARTHROSCOPES receive FDA 510(k) clearance?

KSEA C-MOUNT ARTHROSCOPES received FDA 510(k) clearance on 1998-12-07, under 510(k) number K983142.

Who is the listed applicant for KSEA C-MOUNT ARTHROSCOPES?

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

What is the FDA product code for KSEA C-MOUNT ARTHROSCOPES?

The FDA product code for KSEA C-MOUNT ARTHROSCOPES is HRX.

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Other records listing Karl Storz Endoscopy 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.

K043375FISCH TITANIUM MIDDLE EAR PROSTHESESK030848PERFORATED BIOABSORBABLE INTERFERENCE SCREW MEGAFIXK030009KSEA POWERSHAVER SYSTEM S2K023924AUTOCON II 200 ELECTROSURGICAL GENERATORK023187KSEA SPINOSCOPEK011700MODULITH SLK LITHOTRIPTER

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Related Devices (Code: HRX)

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.

K260203Fule Vertebroplasty Balloon CatheterBeijing Fule Science & Technology Development Co., Ltd.K254103HOPKINS Telescopes for ArthroscopyKarl Storz SE & CO. KGK252790Digital ClarusScope System and Digital NeuroPEN SystemClarus Medical, LLCK253523Freedom DS™ Decompression SystemSpinal SimplicityK252546VantageTM Lumbar Decompression KitAllevion Medical, LLCK253217MiiS 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.

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