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AEROSYNC FOR AERODR SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K120477
510(k) Type
Traditional
Applicant
KONICA MINOLTA MEDICAL & GRAPHIC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/9/2012
Days to Decision
53 days
Submission Type
Summary

AEROSYNC FOR AERODR SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K120477
510(k) Type
Traditional
Applicant
KONICA MINOLTA MEDICAL & GRAPHIC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/9/2012
Days to Decision
53 days
Submission Type
Summary