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NEW IOWA MOTILITY IMPLANT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K900080
510(k) Type
Traditional
Applicant
OCULO PLASTIK, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
3/23/1990
Days to Decision
78 days

NEW IOWA MOTILITY IMPLANT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K900080
510(k) Type
Traditional
Applicant
OCULO PLASTIK, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
3/23/1990
Days to Decision
78 days