Last synced on 25 January 2026 at 3:41 am

PERI-PUSHER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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