SKYTRON MODEL 1100 AND MODEL 142— 510(k) K900290
Substantially EquivalentSkytron, Div. the Kmw Group, Inc.
FDA 510(k) clearance K900290 for SKYTRON MODEL 1100 AND MODEL 142, Substantially Equivalent on 1990-02-20. Applicant: Skytron, Div. the Kmw Group, Inc.. Device class: 1.
Clearance details
- Applicant
- Skytron, Div. the Kmw Group, Inc.
- Product code
- Code JEA
- Device class
- Class 1
- Regulation
- 21 CFR 878.4960
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Grand Rapids, MI, US
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