Last synced on 18 April 2025 at 11:05 pm

WRIST TYPE DIGITAL BLOOD PRESSURE MONITOR, MODEL HD-303S

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K991688
510(k) Type
Traditional
Applicant
JAWON MEDICAL CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/1/1999
Days to Decision
15 days
Submission Type
Summary

WRIST TYPE DIGITAL BLOOD PRESSURE MONITOR, MODEL HD-303S

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K991688
510(k) Type
Traditional
Applicant
JAWON MEDICAL CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/1/1999
Days to Decision
15 days
Submission Type
Summary