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FDA 510(k)

ELECTROSTIMULATOR MODEL 808

K-Number: K880426 · 1988-09-19

ApplicantCornell Enterprises Co., Inc.
Decision Date1988-09-19
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ELECTROSTIMULATOR MODEL 808 is the device name listed in this FDA 510(k) record. The listed applicant is Cornell Enterprises Co., Inc.. It received FDA 510(k) clearance on 1988-09-19 under 510(k) number K880426. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTROSTIMULATOR MODEL 808?

ELECTROSTIMULATOR MODEL 808 is a medical device that received FDA 510(k) clearance on 1988-09-19. The listed applicant is Cornell Enterprises Co., Inc.. The 510(k) number is K880426.

When did ELECTROSTIMULATOR MODEL 808 receive FDA 510(k) clearance?

ELECTROSTIMULATOR MODEL 808 received FDA 510(k) clearance on 1988-09-19, under 510(k) number K880426.

Who is the listed applicant for ELECTROSTIMULATOR MODEL 808?

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

What is the FDA product code for ELECTROSTIMULATOR MODEL 808?

The FDA product code for ELECTROSTIMULATOR MODEL 808 is GZJ.

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Related Devices (Code: GZJ)

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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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