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HYDROCISION ARTHROJET SYSTEM WITH CAUTERY

Page Type
Cleared 510(K)
510(k) Number
K993009
510(k) Type
Traditional
Applicant
HYDROCISION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/25/1999
Days to Decision
48 days
Submission Type
Summary

HYDROCISION ARTHROJET SYSTEM WITH CAUTERY

Page Type
Cleared 510(K)
510(k) Number
K993009
510(k) Type
Traditional
Applicant
HYDROCISION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/25/1999
Days to Decision
48 days
Submission Type
Summary