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FDA 510(k)

CO2 FOR ARTHROSCOPY

K-Number: K852592 · 1985-08-09

ApplicantThe Anspach Effort, Inc.
Decision Date1985-08-09
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CO2 FOR ARTHROSCOPY is the device name listed in this FDA 510(k) record. The listed applicant is The Anspach Effort, Inc.. It received FDA 510(k) clearance on 1985-08-09 under 510(k) number K852592. 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 CO2 FOR ARTHROSCOPY?

CO2 FOR ARTHROSCOPY is a medical device that received FDA 510(k) clearance on 1985-08-09. The listed applicant is The Anspach Effort, Inc.. The 510(k) number is K852592.

When did CO2 FOR ARTHROSCOPY receive FDA 510(k) clearance?

CO2 FOR ARTHROSCOPY received FDA 510(k) clearance on 1985-08-09, under 510(k) number K852592.

Who is the listed applicant for CO2 FOR ARTHROSCOPY?

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

What is the FDA product code for CO2 FOR ARTHROSCOPY?

The FDA product code for CO2 FOR ARTHROSCOPY is HRX.

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Other records listing The Anspach Effort, Inc. as applicant

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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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