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CELESTIN DILATOR

Page Type
Cleared 510(K)
510(k) Number
K812289
510(k) Type
Traditional
Applicant
INMED CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/1/1981
Days to Decision
19 days

CELESTIN DILATOR

Page Type
Cleared 510(K)
510(k) Number
K812289
510(k) Type
Traditional
Applicant
INMED CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/1/1981
Days to Decision
19 days