Last synced on 12 October 2025 at 8:21 pm

Patient Monitoring Cables

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K203635
510(k) Type
Traditional
Applicant
JKH USA, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/5/2021
Days to Decision
53 days
Submission Type
Summary

Patient Monitoring Cables

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K203635
510(k) Type
Traditional
Applicant
JKH USA, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/5/2021
Days to Decision
53 days
Submission Type
Summary