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FDA 510(k)

MYELOTEC VIDEO GUIDED CATHETER

K-Number: K980734 · 1998-08-11

ApplicantMyelotec, Inc.
Decision Date1998-08-11
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MYELOTEC VIDEO GUIDED CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Myelotec, Inc.. It received FDA 510(k) clearance on 1998-08-11 under 510(k) number K980734. 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 MYELOTEC VIDEO GUIDED CATHETER?

MYELOTEC VIDEO GUIDED CATHETER is a medical device that received FDA 510(k) clearance on 1998-08-11. The listed applicant is Myelotec, Inc.. The 510(k) number is K980734.

When did MYELOTEC VIDEO GUIDED CATHETER receive FDA 510(k) clearance?

MYELOTEC VIDEO GUIDED CATHETER received FDA 510(k) clearance on 1998-08-11, under 510(k) number K980734.

Who is the listed applicant for MYELOTEC VIDEO GUIDED CATHETER?

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

What is the FDA product code for MYELOTEC VIDEO GUIDED CATHETER?

The FDA product code for MYELOTEC VIDEO GUIDED CATHETER is HRX.

Related Clinical Trials

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Other records listing Myelotec, 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.

K960194MYELOTEC MYELOSCOPE

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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