TENZCARE(TM) SNAP ELECTRODE 6867
K-Number: K864973 · 1987-01-20
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Device Summary
Frequently Asked Questions
What is the TENZCARE(TM) SNAP ELECTRODE 6867?
TENZCARE(TM) SNAP ELECTRODE 6867 is a medical device that received FDA 510(k) clearance on 1987-01-20. The listed applicant is 3M Company. The 510(k) number is K864973.
When did TENZCARE(TM) SNAP ELECTRODE 6867 receive FDA 510(k) clearance?
TENZCARE(TM) SNAP ELECTRODE 6867 received FDA 510(k) clearance on 1987-01-20, under 510(k) number K864973.
Who is the listed applicant for TENZCARE(TM) SNAP ELECTRODE 6867?
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 TENZCARE(TM) SNAP ELECTRODE 6867?
The FDA product code for TENZCARE(TM) SNAP ELECTRODE 6867 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 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: 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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