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ORIMS DIGITAL ANGIOGRAPHY SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K952480
510(k) Type
Traditional
Applicant
MIDWEST OPHTHALMIC INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/25/1995
Days to Decision
87 days
Submission Type
Statement

ORIMS DIGITAL ANGIOGRAPHY SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K952480
510(k) Type
Traditional
Applicant
MIDWEST OPHTHALMIC INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/25/1995
Days to Decision
87 days
Submission Type
Statement