Last synced on 9 May 2025 at 11:05 pm

MAMMOTOME HH HAND-HELD PROBE, VACUUM SET, CONTROL MODULE, HH HAND-HELD HOLSTER AND CABLES, SOFTWARE PACKAGE, FOOTSWITCH,

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K991980
510(k) Type
Traditional
Applicant
ETHICON ENDO-SURGERY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/17/1999
Days to Decision
64 days
Submission Type
Summary

MAMMOTOME HH HAND-HELD PROBE, VACUUM SET, CONTROL MODULE, HH HAND-HELD HOLSTER AND CABLES, SOFTWARE PACKAGE, FOOTSWITCH,

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K991980
510(k) Type
Traditional
Applicant
ETHICON ENDO-SURGERY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/17/1999
Days to Decision
64 days
Submission Type
Summary