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FDA 510(k)

MEDITRON COMBINATION GENERATOR CG-2000

K-Number: K912182 · 1991-09-06

ApplicantMedical Devices, Inc.
Decision Date1991-09-06
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MEDITRON COMBINATION GENERATOR CG-2000 is the device name listed in this FDA 510(k) record. The listed applicant is Medical Devices, Inc.. It received FDA 510(k) clearance on 1991-09-06 under 510(k) number K912182. 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 MEDITRON COMBINATION GENERATOR CG-2000?

MEDITRON COMBINATION GENERATOR CG-2000 is a medical device that received FDA 510(k) clearance on 1991-09-06. The listed applicant is Medical Devices, Inc.. The 510(k) number is K912182.

When did MEDITRON COMBINATION GENERATOR CG-2000 receive FDA 510(k) clearance?

MEDITRON COMBINATION GENERATOR CG-2000 received FDA 510(k) clearance on 1991-09-06, under 510(k) number K912182.

Who is the listed applicant for MEDITRON COMBINATION GENERATOR CG-2000?

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

What is the FDA product code for MEDITRON COMBINATION GENERATOR CG-2000?

The FDA product code for MEDITRON COMBINATION GENERATOR CG-2000 is GEI.

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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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