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FDA 510(k)

ELECTRO SURGERY SYSTEM

K-Number: K841165 · 1984-06-05

ApplicantMicro-Aire Surgical Instruments, Inc.
Decision Date1984-06-05
Product CodeGEY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ELECTRO SURGERY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Micro-Aire Surgical Instruments, Inc.. It received FDA 510(k) clearance on 1984-06-05 under 510(k) number K841165. 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 ELECTRO SURGERY SYSTEM?

ELECTRO SURGERY SYSTEM is a medical device that received FDA 510(k) clearance on 1984-06-05. The listed applicant is Micro-Aire Surgical Instruments, Inc.. The 510(k) number is K841165.

When did ELECTRO SURGERY SYSTEM receive FDA 510(k) clearance?

ELECTRO SURGERY SYSTEM received FDA 510(k) clearance on 1984-06-05, under 510(k) number K841165.

Who is the listed applicant for ELECTRO SURGERY SYSTEM?

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

What is the FDA product code for ELECTRO SURGERY SYSTEM?

The FDA product code for ELECTRO SURGERY SYSTEM is GEY.

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Other records listing Micro-Aire Surgical Instruments, 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.

K904949A.O. SYNTHES,TAP(REPLACEMENT)VARIOUS MODEL NUMBERSK903713OSTEOTOME MODEL NUMBERS 2500-228 & 2500-229K902676MICROGUARD, ORTHOPEDIC PIN PROTECTORSK903650OSCILLATING SAW BLADES # SO-305,MO-305 AND ZO-305K903664MICRO-AIRE WIRE PASS AND CRANIOTOME DRILLK901967DENDIA WERK BURS AND CUTTING DISCS

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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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