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FDA 510(k)

ELECTROSURGICAL CUTTING & COAGULATION DEVICE/ACCES

K-Number: K854231 · 1986-05-02

ApplicantClinical Technology Corp.
Decision Date1986-05-02
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ELECTROSURGICAL CUTTING & COAGULATION DEVICE/ACCES is the device name listed in this FDA 510(k) record. The listed applicant is Clinical Technology Corp.. It received FDA 510(k) clearance on 1986-05-02 under 510(k) number K854231. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTROSURGICAL CUTTING & COAGULATION DEVICE/ACCES?

ELECTROSURGICAL CUTTING & COAGULATION DEVICE/ACCES is a medical device that received FDA 510(k) clearance on 1986-05-02. The listed applicant is Clinical Technology Corp.. The 510(k) number is K854231.

When did ELECTROSURGICAL CUTTING & COAGULATION DEVICE/ACCES receive FDA 510(k) clearance?

ELECTROSURGICAL CUTTING & COAGULATION DEVICE/ACCES received FDA 510(k) clearance on 1986-05-02, under 510(k) number K854231.

Who is the listed applicant for ELECTROSURGICAL CUTTING & COAGULATION DEVICE/ACCES?

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

What is the FDA product code for ELECTROSURGICAL CUTTING & COAGULATION DEVICE/ACCES?

The FDA product code for ELECTROSURGICAL CUTTING & COAGULATION DEVICE/ACCES is GEI.

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Other records listing Clinical Technology Corp. 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.

K925080TEK-LUBEK872867BIOSIGNK880166BOVIE ULTRASONIC SURGICAL ASPIRATOR, MODEL ME2000K872705BOVIE 400-CT ELECTROSURGICAL GENERATOR (UNIT)K855138BOVIE ULTRASONIC SURGICAL SYSTEMK853507STERI-GRIP

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Related Devices (Code: GEI)

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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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