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LATERAL ANGIOGRAPHIC C-ARM SUPPORT MH-400

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K033184
510(k) Type
Traditional
Applicant
SHIMADZU CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/9/2003
Days to Decision
69 days
Submission Type
Statement

LATERAL ANGIOGRAPHIC C-ARM SUPPORT MH-400

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K033184
510(k) Type
Traditional
Applicant
SHIMADZU CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/9/2003
Days to Decision
69 days
Submission Type
Statement