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..
Clearance details
- Applicant
- Skytron, Div. the Kmw Group, Inc.
- Product code
- Code JEA
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Grand Rapids, MI, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.