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PORTASCAN BLADDER SCANNER, MODEL PA00146

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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