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MODIFICATION TO:LAPAROSCOPIC/ENDOSCOPIC INSTRUMENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010779
510(k) Type
Special
Applicant
GIBBONS SURGICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/10/2001
Days to Decision
26 days
Submission Type
Statement

MODIFICATION TO:LAPAROSCOPIC/ENDOSCOPIC INSTRUMENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010779
510(k) Type
Special
Applicant
GIBBONS SURGICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/10/2001
Days to Decision
26 days
Submission Type
Statement