Last synced on 14 November 2025 at 11:06 pm

VITALMAX 840 SERIES

Page Type
Cleared 510(K)
510(k) Number
K914164
510(k) Type
Traditional
Applicant
PACE TECH MEDICAL MONITORS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/9/1993
Days to Decision
570 days
Submission Type
Statement

VITALMAX 840 SERIES

Page Type
Cleared 510(K)
510(k) Number
K914164
510(k) Type
Traditional
Applicant
PACE TECH MEDICAL MONITORS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/9/1993
Days to Decision
570 days
Submission Type
Statement