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PORGES STEPPED NEOPLEX DILATOR

Page Type
Cleared 510(K)
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)
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