MYOCARE PLUS DUAL CHANNEL STIMULATOR— 510(k) K851046
Substantially Equivalent for Some Indications3M Company
FDA 510(k) clearance K851046 for MYOCARE PLUS DUAL CHANNEL STIMULATOR, Substantially Equivalent for Some Indications on 1985-07-01. Applicant: 3M Company. Device class: 2.
Clearance details
- Applicant
- 3M Company
- Product code
- Code IPF
- Device class
- Class 2
- Regulation
- 21 CFR 890.5850
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent for Some Indications
- Clearance type
- Traditional
- Location
- Cottae Grove, MN, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.