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PORTASCAN BLADDER SCANNER, MODEL PA00146

Page Type
Cleared 510(K)
510(k) Number
K033906
510(k) Type
Traditional
Applicant
MEDIWATCH PLC
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
12/24/2003
Days to Decision
7 days
Submission Type
Statement

PORTASCAN BLADDER SCANNER, MODEL PA00146

Page Type
Cleared 510(K)
510(k) Number
K033906
510(k) Type
Traditional
Applicant
MEDIWATCH PLC
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
12/24/2003
Days to Decision
7 days
Submission Type
Statement