Last synced on 14 November 2025 at 11:06 pm

GNOMOS STEREOTACTIC DEVICE

Page Type
Cleared 510(K)
510(k) Number
K901670
510(k) Type
Traditional
Applicant
MEDICAL EQUIPMENT DEVELOPMENT CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/3/1990
Days to Decision
84 days

GNOMOS STEREOTACTIC DEVICE

Page Type
Cleared 510(K)
510(k) Number
K901670
510(k) Type
Traditional
Applicant
MEDICAL EQUIPMENT DEVELOPMENT CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/3/1990
Days to Decision
84 days