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INSTRUMENT, ULTRASONIC, SCALPEL

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K990362
510(k) Type
Traditional
Applicant
Ethicon Endo-Surgery, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/17/1999
Days to Decision
224 days
Submission Type
Summary

INSTRUMENT, ULTRASONIC, SCALPEL

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K990362
510(k) Type
Traditional
Applicant
Ethicon Endo-Surgery, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/17/1999
Days to Decision
224 days
Submission Type
Summary