STIMEL-03— 510(k) K130424
Substantially EquivalentStimel, Ltd.
FDA 510(k) clearance K130424 for STIMEL-03, Substantially Equivalent on 2013-07-11. Applicant: Stimel, Ltd.. Device class: 2.
Clearance details
- Applicant
- Stimel, Ltd.
- Product code
- Code IPF
- Device class
- Class 2
- Regulation
- 21 CFR 890.5850
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Monroe, CT, US
Recent devices under product code IPF
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