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MAGGI SERIES ULTRA. NEEDLE, BIOPSY/CATHETER GUIDES

Page Type
Cleared 510(K)
510(k) Number
K882383
510(k) Type
Traditional
Applicant
CIVCO MEDICAL INSTRUMENTS CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/28/1988
Days to Decision
172 days

MAGGI SERIES ULTRA. NEEDLE, BIOPSY/CATHETER GUIDES

Page Type
Cleared 510(K)
510(k) Number
K882383
510(k) Type
Traditional
Applicant
CIVCO MEDICAL INSTRUMENTS CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/28/1988
Days to Decision
172 days