Last synced on 2 May 2025 at 11:05 pm

NEONATAL ECG ELECTRODE, M203KEN

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092744
510(k) Type
Traditional
Applicant
R & D MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/10/2009
Days to Decision
93 days
Submission Type
Summary

NEONATAL ECG ELECTRODE, M203KEN

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092744
510(k) Type
Traditional
Applicant
R & D MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/10/2009
Days to Decision
93 days
Submission Type
Summary