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PERI-PUSHER

Page Type
Cleared 510(K)
510(k) Number
K953046
510(k) Type
Traditional
Applicant
DIACOR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/22/1995
Days to Decision
84 days
Submission Type
Statement

PERI-PUSHER

Page Type
Cleared 510(K)
510(k) Number
K953046
510(k) Type
Traditional
Applicant
DIACOR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/22/1995
Days to Decision
84 days
Submission Type
Statement