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SHIMADZU IMAGE AMPLIFIER IA-12LM SERIES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K936236
510(k) Type
Traditional
Applicant
SHIMADZU MEDICAL SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/11/1995
Days to Decision
497 days
Submission Type
Statement

SHIMADZU IMAGE AMPLIFIER IA-12LM SERIES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K936236
510(k) Type
Traditional
Applicant
SHIMADZU MEDICAL SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/11/1995
Days to Decision
497 days
Submission Type
Statement