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PERSONNA PLUS SAFETY SCALPEL SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032242
510(k) Type
Traditional
Applicant
OMI MANUFACTURING PTY., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/23/2003
Days to Decision
64 days
Submission Type
Summary

PERSONNA PLUS SAFETY SCALPEL SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032242
510(k) Type
Traditional
Applicant
OMI MANUFACTURING PTY., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/23/2003
Days to Decision
64 days
Submission Type
Summary