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TOSHIBA RTP9211J-G11, J-ADVANCED IMAGE INTENSIFIER (I.I.)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K993038
510(k) Type
Traditional
Applicant
TOSHIBA AMERICA MEDICAL SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/7/1999
Days to Decision
27 days
Submission Type
Summary

TOSHIBA RTP9211J-G11, J-ADVANCED IMAGE INTENSIFIER (I.I.)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K993038
510(k) Type
Traditional
Applicant
TOSHIBA AMERICA MEDICAL SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/7/1999
Days to Decision
27 days
Submission Type
Summary