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VERTEX DIGITAL SUBSTRATION KIT

Page Type
Cleared 510(K)
510(k) Number
K830637
510(k) Type
Traditional
Applicant
PROFESSIONAL MEDICAL SERVICES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/24/1983
Days to Decision
23 days

VERTEX DIGITAL SUBSTRATION KIT

Page Type
Cleared 510(K)
510(k) Number
K830637
510(k) Type
Traditional
Applicant
PROFESSIONAL MEDICAL SERVICES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/24/1983
Days to Decision
23 days