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HYDROCISION ARTHROJET SYSTEM WITH CAUTERY AND BURR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002764
510(k) Type
Traditional
Applicant
HYDROCISION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/24/2000
Days to Decision
80 days
Submission Type
Summary

HYDROCISION ARTHROJET SYSTEM WITH CAUTERY AND BURR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002764
510(k) Type
Traditional
Applicant
HYDROCISION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/24/2000
Days to Decision
80 days
Submission Type
Summary