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AVITA BPM1 SERIES (WRIST TYPE) BLOOD PRESSURE METER (OR MONITOR)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030230
510(k) Type
Traditional
Applicant
AVITA CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/23/2003
Days to Decision
121 days
Submission Type
Summary

AVITA BPM1 SERIES (WRIST TYPE) BLOOD PRESSURE METER (OR MONITOR)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030230
510(k) Type
Traditional
Applicant
AVITA CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/23/2003
Days to Decision
121 days
Submission Type
Summary