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FDA 510(k)

ELECTRIC WIRE DRIVER, MODEL 2640E

K-Number: K930205 · 1993-08-02

ApplicantMicro Surgical Instruments Corp.
Decision Date1993-08-02
Product CodeHXJ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ELECTRIC WIRE DRIVER, MODEL 2640E 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 1993-08-02 under 510(k) number K930205. The device is classified under product code HXJ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTRIC WIRE DRIVER, MODEL 2640E?

ELECTRIC WIRE DRIVER, MODEL 2640E is a medical device that received FDA 510(k) clearance on 1993-08-02. The listed applicant is Micro Surgical Instruments Corp.. The 510(k) number is K930205.

When did ELECTRIC WIRE DRIVER, MODEL 2640E receive FDA 510(k) clearance?

ELECTRIC WIRE DRIVER, MODEL 2640E received FDA 510(k) clearance on 1993-08-02, under 510(k) number K930205.

Who is the listed applicant for ELECTRIC WIRE DRIVER, MODEL 2640E?

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 ELECTRIC WIRE DRIVER, MODEL 2640E?

The FDA product code for ELECTRIC WIRE DRIVER, MODEL 2640E is HXJ.

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Other records listing Micro Surgical Instruments Corp. as applicant

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K931395SERIES 5000 BATTERY POWERED INSTRUMENT SYSTEMK932492IMPLANTOLOGY MODULE, MODEL 2175K914998MICROAIRE(R) FACIAL BONE PLATING SYSTEMK915139MODEL 2250-000 ZIMMER STYLE SAGITTAL SAW MODULEK914346DRILL MODULES MODELS 2116/2117K913369MICRO-AIRE MODEL 2060

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Related Devices (Code: HXJ)

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.

K964953IN-TAC BONE ANCHOR SYSTEMInfluence, Inc.K962372UROTAC BONE ANCHOR INSERTERInfluence, Inc.K834515FIXATION STAPLE KIT - DLIDE HAMMERStryker Corp.K830456STAPLE INSERTER-EXTRACTOR FOR ARTHROSInstrument Makar, Inc.K830255OSTEOTOMY BONE STAPLETechmedica, 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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