Tenzcare(Tm) Snap Electrode 6867
FDA 510(k) K864973 · 3M Company
510(k) numberK864973
Submission
- Device name
- Tenzcare(Tm) Snap Electrode 6867
- Applicant
- 3M Company
Cottae Grove, MN, US - Received
- December 19, 1986
- Decision date
- January 20, 1987
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
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Questions and answers
When was Tenzcare(Tm) Snap Electrode 6867 cleared by the FDA?
Tenzcare(Tm) Snap Electrode 6867 (K864973) received a 510(k) decision of Substantially Equivalent on January 20, 1987, 32 days after the submission was received.
What is the product code of K864973?
The FDA product code is GXY – Electrode, Cutaneous, a Class II (moderate risk) device regulated under 21 CFR 882.1320.