Last synced on 16 August 2024 at 11:05 pm

VITALMAX 2000 ECG MONITOR W/NON-INVASIVE BLOOD-PRE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K901612
510(k) Type
Traditional
Applicant
PACE TECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/30/1990
Days to Decision
24 days

VITALMAX 2000 ECG MONITOR W/NON-INVASIVE BLOOD-PRE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K901612
510(k) Type
Traditional
Applicant
PACE TECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/30/1990
Days to Decision
24 days