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FDA 510(k)

BLADES, WHISKERS, TRIMMERS, CUTTERS, AND BURS

K-Number: K912108 · 1991-07-02

ApplicantMicroaire Advanced Surgical Products
Decision Date1991-07-02
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

BLADES, WHISKERS, TRIMMERS, CUTTERS, AND BURS is the device name listed in this FDA 510(k) record. The listed applicant is Microaire Advanced Surgical Products. It received FDA 510(k) clearance on 1991-07-02 under 510(k) number K912108. 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 BLADES, WHISKERS, TRIMMERS, CUTTERS, AND BURS?

BLADES, WHISKERS, TRIMMERS, CUTTERS, AND BURS is a medical device that received FDA 510(k) clearance on 1991-07-02. The listed applicant is Microaire Advanced Surgical Products. The 510(k) number is K912108.

When did BLADES, WHISKERS, TRIMMERS, CUTTERS, AND BURS receive FDA 510(k) clearance?

BLADES, WHISKERS, TRIMMERS, CUTTERS, AND BURS received FDA 510(k) clearance on 1991-07-02, under 510(k) number K912108.

Who is the listed applicant for BLADES, WHISKERS, TRIMMERS, CUTTERS, AND BURS?

The FDA 510(k) record lists Microaire Advanced Surgical Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BLADES, WHISKERS, TRIMMERS, CUTTERS, AND BURS?

The FDA product code for BLADES, WHISKERS, TRIMMERS, CUTTERS, AND BURS is HRX.

Related Clinical Trials

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Other records listing Microaire Advanced Surgical Products 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.

K912767FIBER OPTIC UNIVERAL CABLES, SCOPE ADAP., LT.SOURC

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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