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QUILL CATHETER GUIDE

Page Type
Cleared 510(K)
510(k) Number
K823303
510(k) Type
Traditional
Applicant
MEDIGROUP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/1983
Days to Decision
82 days

QUILL CATHETER GUIDE

Page Type
Cleared 510(K)
510(k) Number
K823303
510(k) Type
Traditional
Applicant
MEDIGROUP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/1983
Days to Decision
82 days