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FDA 510(k)

TNCO, INC. ARTHROSCOPIC SURGICAL INSTRUMENTS

K-Number: K940554 · 1994-06-29

ApplicantTnco, Inc.
Decision Date1994-06-29
Product CodeHRX
Advisory CommitteeOR
DecisionUnknown

Device Summary

TNCO, INC. ARTHROSCOPIC SURGICAL INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Tnco, Inc.. It received FDA 510(k) clearance on 1994-06-29 under 510(k) number K940554. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the TNCO, INC. ARTHROSCOPIC SURGICAL INSTRUMENTS?

TNCO, INC. ARTHROSCOPIC SURGICAL INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1994-06-29. The listed applicant is Tnco, Inc.. The 510(k) number is K940554.

When did TNCO, INC. ARTHROSCOPIC SURGICAL INSTRUMENTS receive FDA 510(k) clearance?

TNCO, INC. ARTHROSCOPIC SURGICAL INSTRUMENTS received FDA 510(k) clearance on 1994-06-29, under 510(k) number K940554.

Who is the listed applicant for TNCO, INC. ARTHROSCOPIC SURGICAL INSTRUMENTS?

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

What is the FDA product code for TNCO, INC. ARTHROSCOPIC SURGICAL INSTRUMENTS?

The FDA product code for TNCO, INC. ARTHROSCOPIC SURGICAL INSTRUMENTS is HRX.

Related Clinical Trials

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Other records listing Tnco, 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.

K943958MONOPOLAR ENDOSCOPIC REPOSABLE TIP SURGICAL INSTRUMENTSK940552MONOPOLAR SURGICAL INSTRUMENTSK940551ENDOSCOPIC SURGICAL INSTRUMENTS

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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