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ENTEC REFLEX WAND 55, MODEL E4055-01, E4045-01

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000778
510(k) Type
Traditional
Applicant
ARTHROCARE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/3/2000
Days to Decision
54 days
Submission Type
Summary

ENTEC REFLEX WAND 55, MODEL E4055-01, E4045-01

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000778
510(k) Type
Traditional
Applicant
ARTHROCARE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/3/2000
Days to Decision
54 days
Submission Type
Summary