ARTROMOT K2 CPM— 510(k) K931555
Substantially EquivalentOrmed Mfg., Inc.
FDA 510(k) clearance K931555 for ARTROMOT K2 CPM, Substantially Equivalent on 1994-01-31. Applicant: Ormed Mfg., Inc.. Device class: 1.
Clearance details
- Applicant
- Ormed Mfg., Inc.
- Product code
- Code BXB
- Device class
- Class 1
- Regulation
- 21 CFR 890.5380
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Concord, CA, US
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