Last synced on 18 April 2025 at 11:05 pm

HYDROCISION ARTHROJET SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K982266
510(k) Type
Traditional
Applicant
HYDROCISION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/25/1998
Days to Decision
88 days
Submission Type
Summary

HYDROCISION ARTHROJET SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K982266
510(k) Type
Traditional
Applicant
HYDROCISION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/25/1998
Days to Decision
88 days
Submission Type
Summary