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KONICA LD-4500 LASER DIGITIZER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K933830
510(k) Type
Traditional
Applicant
KONICA MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/14/1993
Days to Decision
131 days
Submission Type
Statement

KONICA LD-4500 LASER DIGITIZER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K933830
510(k) Type
Traditional
Applicant
KONICA MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/14/1993
Days to Decision
131 days
Submission Type
Statement