CUSHMAN MANUFACTURING, INC. ULTRA 6.0.— 510(k) K960802
Substantially EquivalentCushman Mfg., Inc.
FDA 510(k) clearance K960802 for CUSHMAN MANUFACTURING, INC. ULTRA 6.0., Substantially Equivalent on 1996-06-18. Applicant: Cushman Mfg., Inc.. Device class: 2.
Clearance details
- Applicant
- Cushman Mfg., Inc.
- Product code
- Code IMI
- Device class
- Class 2
- Regulation
- 21 CFR 890.5300
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Long Beach, CA, US
Recent devices under product code IMI
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