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DEFOGGING HEATED ENDOSCOPE LENS PROTECTOR (DHELP); DEFOGGING ENDOSCOPE LENS PROTECTOR (DELP)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K062779
510(k) Type
Traditional
Applicant
NEW WAVE SURGICAL CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/5/2006
Days to Decision
17 days
Submission Type
Summary