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ESPI MICRO GRASPER,DOUBLE-ACTION,INSULATED,#8250-N

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K903600
510(k) Type
Traditional
Applicant
DIXON MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/17/1990
Days to Decision
70 days

ESPI MICRO GRASPER,DOUBLE-ACTION,INSULATED,#8250-N

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K903600
510(k) Type
Traditional
Applicant
DIXON MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/17/1990
Days to Decision
70 days