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FDA 510(k)

ESA ELECTROSURGICAL ARTHROSCOPY GENERA

K-Number: K830499 · 1983-03-17

ApplicantConcept, Inc.
Decision Date1983-03-17
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ESA ELECTROSURGICAL ARTHROSCOPY GENERA is the device name listed in this FDA 510(k) record. The listed applicant is Concept, Inc.. It received FDA 510(k) clearance on 1983-03-17 under 510(k) number K830499. 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 ESA ELECTROSURGICAL ARTHROSCOPY GENERA?

ESA ELECTROSURGICAL ARTHROSCOPY GENERA is a medical device that received FDA 510(k) clearance on 1983-03-17. The listed applicant is Concept, Inc.. The 510(k) number is K830499.

When did ESA ELECTROSURGICAL ARTHROSCOPY GENERA receive FDA 510(k) clearance?

ESA ELECTROSURGICAL ARTHROSCOPY GENERA received FDA 510(k) clearance on 1983-03-17, under 510(k) number K830499.

Who is the listed applicant for ESA ELECTROSURGICAL ARTHROSCOPY GENERA?

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

What is the FDA product code for ESA ELECTROSURGICAL ARTHROSCOPY GENERA?

The FDA product code for ESA ELECTROSURGICAL ARTHROSCOPY GENERA is HRX.

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Other records listing Concept, 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.

K912640CONCEPT ENDOSTEAL FIXATION DEVICEK912957CONCEPT MICROMILLK896648CONCEPT UNICOMPARTMENTAL KNEE SYSTEMK894929STAPLE FIXATION SYSTEMK892376INTRAVISION(TM) ARTHROSCOPE SYSTEM (ADD'L APPLI.)K891109PANDA(R) NEEDLE CATHETER JEJUNOSTOMY TUBE

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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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