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FDA 510(k)

ALL PURPOSE ELECTROSURGICAL GENERATOR

K-Number: K841483 · 1984-10-23

ApplicantConcept, Inc.
Decision Date1984-10-23
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ALL PURPOSE ELECTROSURGICAL GENERATOR is the device name listed in this FDA 510(k) record. The listed applicant is Concept, Inc.. It received FDA 510(k) clearance on 1984-10-23 under 510(k) number K841483. 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 ALL PURPOSE ELECTROSURGICAL GENERATOR?

ALL PURPOSE ELECTROSURGICAL GENERATOR is a medical device that received FDA 510(k) clearance on 1984-10-23. The listed applicant is Concept, Inc.. The 510(k) number is K841483.

When did ALL PURPOSE ELECTROSURGICAL GENERATOR receive FDA 510(k) clearance?

ALL PURPOSE ELECTROSURGICAL GENERATOR received FDA 510(k) clearance on 1984-10-23, under 510(k) number K841483.

Who is the listed applicant for ALL PURPOSE ELECTROSURGICAL GENERATOR?

The FDA 510(k) record lists Concept, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ALL PURPOSE ELECTROSURGICAL GENERATOR?

The FDA product code for ALL PURPOSE ELECTROSURGICAL GENERATOR is GEI.

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Other records listing Concept, 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.

K912640CONCEPT ENDOSTEAL FIXATION DEVICEK912957CONCEPT MICROMILLK896648CONCEPT UNICOMPARTMENTAL KNEE SYSTEMK894929STAPLE FIXATION SYSTEMK892376INTRAVISION(TM) ARTHROSCOPE SYSTEM (ADD'L APPLI.)K891109PANDA(R) NEEDLE CATHETER JEJUNOSTOMY TUBE

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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