MODEL 9000 AT ANKLE CPM DEVICE— 510(k) K902707
Substantially EquivalentSutter Corp.
FDA 510(k) clearance K902707 for MODEL 9000 AT ANKLE CPM DEVICE, Substantially Equivalent on 1990-07-25. Applicant: Sutter Corp..
Clearance details
- Applicant
- Sutter Corp.
- Product code
- Code BXB
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- San Diego, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.