Last synced on 14 November 2025 at 11:06 pm

TUBING BLOOD FLOW METER MODEL NUMBER HD-800

Page Type
Cleared 510(K)
510(k) Number
K982986
510(k) Type
Traditional
Applicant
KOVEN TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/24/1998
Days to Decision
90 days
Submission Type
Summary

TUBING BLOOD FLOW METER MODEL NUMBER HD-800

Page Type
Cleared 510(K)
510(k) Number
K982986
510(k) Type
Traditional
Applicant
KOVEN TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/24/1998
Days to Decision
90 days
Submission Type
Summary