Last synced on 25 January 2026 at 3:41 am

TN-RD-50

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K932598
510(k) Type
Traditional
Applicant
KEITHLEY INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/3/1994
Days to Decision
371 days
Submission Type
Statement

TN-RD-50

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K932598
510(k) Type
Traditional
Applicant
KEITHLEY INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/3/1994
Days to Decision
371 days
Submission Type
Statement