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POREX ELECTROSURGERY NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K052297
510(k) Type
Traditional
Applicant
POREX SURGICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/28/2006
Days to Decision
217 days
Submission Type
Summary

POREX ELECTROSURGERY NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K052297
510(k) Type
Traditional
Applicant
POREX SURGICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/28/2006
Days to Decision
217 days
Submission Type
Summary