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FDA 510(k)

STIMUCORD EXTERNAL NEURAL STIM. 911A

K-Number: K823530 · 1982-12-15

ApplicantCordis Corp.
Decision Date1982-12-15
Product CodeGZB
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

STIMUCORD EXTERNAL NEURAL STIM. 911A is the device name listed in this FDA 510(k) record. The listed applicant is Cordis Corp.. It received FDA 510(k) clearance on 1982-12-15 under 510(k) number K823530. The device is classified under product code GZB. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STIMUCORD EXTERNAL NEURAL STIM. 911A?

STIMUCORD EXTERNAL NEURAL STIM. 911A is a medical device that received FDA 510(k) clearance on 1982-12-15. The listed applicant is Cordis Corp.. The 510(k) number is K823530.

When did STIMUCORD EXTERNAL NEURAL STIM. 911A receive FDA 510(k) clearance?

STIMUCORD EXTERNAL NEURAL STIM. 911A received FDA 510(k) clearance on 1982-12-15, under 510(k) number K823530.

Who is the listed applicant for STIMUCORD EXTERNAL NEURAL STIM. 911A?

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

What is the FDA product code for STIMUCORD EXTERNAL NEURAL STIM. 911A?

The FDA product code for STIMUCORD EXTERNAL NEURAL STIM. 911A is GZB.

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Related Devices (Code: GZB)

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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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