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PULPDENT RESILUTE II

Page Type
Cleared 510(K)
510(k) Number
K962383
510(k) Type
Traditional
Applicant
PULPDENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/3/1996
Days to Decision
75 days
Submission Type
Summary

PULPDENT RESILUTE II

Page Type
Cleared 510(K)
510(k) Number
K962383
510(k) Type
Traditional
Applicant
PULPDENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/3/1996
Days to Decision
75 days
Submission Type
Summary