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PORGES STEPPED NEOPLEX DILATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K883526
510(k) Type
Traditional
Applicant
PORGES CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/28/1988
Days to Decision
71 days

PORGES STEPPED NEOPLEX DILATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K883526
510(k) Type
Traditional
Applicant
PORGES CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/28/1988
Days to Decision
71 days