SKALPI 3200— 510(k) K946382
Substantially EquivalentWiscco Development, Inc.
FDA 510(k) clearance K946382 for SKALPI 3200, Substantially Equivalent on 1995-05-30. Applicant: Wiscco Development, Inc.. Device class: 1.
Clearance details
- Applicant
- Wiscco Development, Inc.
- Product code
- Code IRO
- Device class
- Class 1
- Regulation
- 21 CFR 890.5975
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- North Hollywood, CA, US
Recent devices under product code IRO
view allData sourced from openFDA. This site is unofficial and independent of the FDA.