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FDA 510(k)

THE CART

K-Number: K872533 · 1987-11-02

ApplicantArthropedics, Inc.
Decision Date1987-11-02
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

THE CART is the device name listed in this FDA 510(k) record. The listed applicant is Arthropedics, Inc.. It received FDA 510(k) clearance on 1987-11-02 under 510(k) number K872533. 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 THE CART?

THE CART is a medical device that received FDA 510(k) clearance on 1987-11-02. The listed applicant is Arthropedics, Inc.. The 510(k) number is K872533.

When did THE CART receive FDA 510(k) clearance?

THE CART received FDA 510(k) clearance on 1987-11-02, under 510(k) number K872533.

Who is the listed applicant for THE CART?

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

What is the FDA product code for THE CART?

The FDA product code for THE CART is HRX.

Other records listing Arthropedics, 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.

K873619ARTHROSCOPIC RETENTION-MANIPULATION SYSTEM (ARMS)K873653MONOPOLAR CAUTERY BLADE TIP #TM-1701K873654MONOPOLAR CAUTERY CONICAL TIP #TM-1702K873655MONOPOLAR CAUTERY RETROGADE TIP #TM-1703K873387VIDEO ARTHROSCOPE, 1.7MM X 55 MMK873711RETROGRADE KNIFE, DISPOSABLE #TM-1613

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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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