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FDA 510(k)

MICRO-AIRE MODEL 2050E/ELEC HANDPIECE/TROTTLELESS

K-Number: K913266 · 1991-10-21

ApplicantMicro Surgical Instruments Corp.
Decision Date1991-10-21
Product CodeGEY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MICRO-AIRE MODEL 2050E/ELEC HANDPIECE/TROTTLELESS is the device name listed in this FDA 510(k) record. The listed applicant is Micro Surgical Instruments Corp.. It received FDA 510(k) clearance on 1991-10-21 under 510(k) number K913266. The device is classified under product code GEY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRO-AIRE MODEL 2050E/ELEC HANDPIECE/TROTTLELESS?

MICRO-AIRE MODEL 2050E/ELEC HANDPIECE/TROTTLELESS is a medical device that received FDA 510(k) clearance on 1991-10-21. The listed applicant is Micro Surgical Instruments Corp.. The 510(k) number is K913266.

When did MICRO-AIRE MODEL 2050E/ELEC HANDPIECE/TROTTLELESS receive FDA 510(k) clearance?

MICRO-AIRE MODEL 2050E/ELEC HANDPIECE/TROTTLELESS received FDA 510(k) clearance on 1991-10-21, under 510(k) number K913266.

Who is the listed applicant for MICRO-AIRE MODEL 2050E/ELEC HANDPIECE/TROTTLELESS?

The FDA 510(k) record lists Micro Surgical Instruments Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MICRO-AIRE MODEL 2050E/ELEC HANDPIECE/TROTTLELESS?

The FDA product code for MICRO-AIRE MODEL 2050E/ELEC HANDPIECE/TROTTLELESS is GEY.

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Other records listing Micro Surgical Instruments Corp. as applicant

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Related Devices (Code: GEY)

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.

K050519ADVANCED TURBO DRIVE SYSTEMLinvatec Corp.K020621ARTHROCARE CONTROLLER; ARTHROCARE CABLE; FOOT CONTROL; POWER CORD; WANDSArthrocare Corp.K012738SYMPHONY GRAFT DELIVERY SYSTEM (GDS)DepuyacromedK972308MEDNEXT 1000 DRILLMednext, Inc.K971941AQUA SPRAYBoyd Industries, Inc.K971782BONE AND MARROW COLLECTION SYSTEM KITBiomedical Ent., Inc.

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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