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IN-ROOM MRC/ MAGNETOM VISION AND IMPACT SYSTEMS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K962927
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/25/1996
Days to Decision
58 days
Submission Type
Summary