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SKYTRON MODEL 1100 AND MODEL 142

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K900290
510(k) Type
Traditional
Applicant
SKYTRON, DIV. THE KMW GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/20/1990
Days to Decision
29 days

SKYTRON MODEL 1100 AND MODEL 142

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K900290
510(k) Type
Traditional
Applicant
SKYTRON, DIV. THE KMW GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/20/1990
Days to Decision
29 days