Last synced on 2 December 2022 at 11:04 pm

MODIFICATION TO K6-I DIAGNOSTIC SYSTEM, MODEL K6-I

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K992694
510(k) Type
Special
Applicant
MYOTRONICS-NOROMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/10/1999
Days to Decision
29 days
Submission Type
Summary

MODIFICATION TO K6-I DIAGNOSTIC SYSTEM, MODEL K6-I

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K992694
510(k) Type
Special
Applicant
MYOTRONICS-NOROMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/10/1999
Days to Decision
29 days
Submission Type
Summary