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SHIMADZU MOBILE X-RAY SYSTEMS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K940294
510(k) Type
Traditional
Applicant
SHIMADZU PRECISION INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/16/1994
Days to Decision
54 days
Submission Type
Statement

SHIMADZU MOBILE X-RAY SYSTEMS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K940294
510(k) Type
Traditional
Applicant
SHIMADZU PRECISION INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/16/1994
Days to Decision
54 days
Submission Type
Statement