Last synced on 27 January 2023 at 11:04 pm

DISPOSABLE UNIPOLAR COAGULATOR PROBE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K921716
510(k) Type
Traditional
Applicant
AMERICAN SURGICAL INSTRUMENTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/8/1993
Days to Decision
578 days
Submission Type
Statement

DISPOSABLE UNIPOLAR COAGULATOR PROBE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K921716
510(k) Type
Traditional
Applicant
AMERICAN SURGICAL INSTRUMENTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/8/1993
Days to Decision
578 days
Submission Type
Statement