Last synced on 14 November 2025 at 11:06 pm

LIFEDOP DOPPLER

Page Type
Cleared 510(K)
510(k) Number
K024197
510(k) Type
Traditional
Applicant
SUMMIT DOPPLER SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/3/2003
Days to Decision
14 days
Submission Type
Summary

LIFEDOP DOPPLER

Page Type
Cleared 510(K)
510(k) Number
K024197
510(k) Type
Traditional
Applicant
SUMMIT DOPPLER SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/3/2003
Days to Decision
14 days
Submission Type
Summary