Last synced on 9 December 2022 at 11:04 pm

Avulsion Forceps

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K183428
510(k) Type
Traditional
Applicant
STERIS Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/16/2019
Days to Decision
126 days
Submission Type
Summary

Avulsion Forceps

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K183428
510(k) Type
Traditional
Applicant
STERIS Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/16/2019
Days to Decision
126 days
Submission Type
Summary