NEUROMOD STIMULATOR MODEL 3723
K-Number: K780186 · 1978-03-02
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Device Summary
Frequently Asked Questions
What is the NEUROMOD STIMULATOR MODEL 3723?
NEUROMOD STIMULATOR MODEL 3723 is a medical device that received FDA 510(k) clearance on 1978-03-02. The listed applicant is Medtronic Vascular. The 510(k) number is K780186.
When did NEUROMOD STIMULATOR MODEL 3723 receive FDA 510(k) clearance?
NEUROMOD STIMULATOR MODEL 3723 received FDA 510(k) clearance on 1978-03-02, under 510(k) number K780186.
Who is the listed applicant for NEUROMOD STIMULATOR MODEL 3723?
The FDA 510(k) record lists Medtronic Vascular as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NEUROMOD STIMULATOR MODEL 3723?
The FDA product code for NEUROMOD STIMULATOR MODEL 3723 is GZJ.
Related Clinical Trials
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.
Other records listing Medtronic Vascular 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.
Related Devices (Code: GZJ)
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.
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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