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MODIFIED MANUFACTURING PROCESS FOR OMIDERM(TM)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K874480
510(k) Type
Traditional
Applicant
OMIKRON SCIENTIFIC, LTD.
Country
Israel
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
2/22/1988
Days to Decision
112 days

MODIFIED MANUFACTURING PROCESS FOR OMIDERM(TM)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K874480
510(k) Type
Traditional
Applicant
OMIKRON SCIENTIFIC, LTD.
Country
Israel
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
2/22/1988
Days to Decision
112 days