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SKYTRON MODEL 860 AND 800 COMP. SURGITA NEURO EQUI

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K900472
510(k) Type
Traditional
Applicant
SKYTRON, DIV. THE KMW GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/4/1990
Days to Decision
216 days

SKYTRON MODEL 860 AND 800 COMP. SURGITA NEURO EQUI

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K900472
510(k) Type
Traditional
Applicant
SKYTRON, DIV. THE KMW GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/4/1990
Days to Decision
216 days