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3M DIGITAL RECORDING AUTOMATIC FILM HANDLING UNIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K912225
510(k) Type
Traditional
Applicant
3M MEDICAL PRODUCTS GROUP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/22/1991
Days to Decision
63 days
Submission Type
Summary

3M DIGITAL RECORDING AUTOMATIC FILM HANDLING UNIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K912225
510(k) Type
Traditional
Applicant
3M MEDICAL PRODUCTS GROUP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/22/1991
Days to Decision
63 days
Submission Type
Summary