3M SCOTCHPLATE II DISPERSIVE ELECTRODE
K-Number: K833364 · 1983-11-29
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Device Summary
Frequently Asked Questions
What is the 3M SCOTCHPLATE II DISPERSIVE ELECTRODE?
3M SCOTCHPLATE II DISPERSIVE ELECTRODE is a medical device that received FDA 510(k) clearance on 1983-11-29. The listed applicant is 3M Company. The 510(k) number is K833364.
When did 3M SCOTCHPLATE II DISPERSIVE ELECTRODE receive FDA 510(k) clearance?
3M SCOTCHPLATE II DISPERSIVE ELECTRODE received FDA 510(k) clearance on 1983-11-29, under 510(k) number K833364.
Who is the listed applicant for 3M SCOTCHPLATE II DISPERSIVE ELECTRODE?
The FDA 510(k) record lists 3M Company as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 3M SCOTCHPLATE II DISPERSIVE ELECTRODE?
The FDA product code for 3M SCOTCHPLATE II DISPERSIVE ELECTRODE is GEI.
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 3M Company 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: GEI)
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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