ELECTRODE, PNS
K-Number: K760312 · 1976-08-04
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Device Summary
Frequently Asked Questions
What is the ELECTRODE, PNS?
ELECTRODE, PNS is a medical device that received FDA 510(k) clearance on 1976-08-04. The listed applicant is Ndm Corp.. The 510(k) number is K760312.
When did ELECTRODE, PNS receive FDA 510(k) clearance?
ELECTRODE, PNS received FDA 510(k) clearance on 1976-08-04, under 510(k) number K760312.
Who is the listed applicant for ELECTRODE, PNS?
The FDA 510(k) record lists Ndm Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ELECTRODE, PNS?
The FDA product code for ELECTRODE, PNS is GXY.
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 Ndm Corp. 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: GXY)
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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