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AX-390SE AUTOMATIC X-RAY FILM PROCESSOR 9586.033

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K931883
510(k) Type
Traditional
Applicant
ALPHATEK CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/23/1993
Days to Decision
131 days
Submission Type
Statement

AX-390SE AUTOMATIC X-RAY FILM PROCESSOR 9586.033

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K931883
510(k) Type
Traditional
Applicant
ALPHATEK CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/23/1993
Days to Decision
131 days
Submission Type
Statement