Last synced on 14 November 2025 at 11:06 pm

HOMMED SENTRY III PATIENT MONITOR SYSTEM WITH CARD READER

Page Type
Cleared 510(K)
510(k) Number
K014025
510(k) Type
Traditional
Applicant
HOMMED LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/9/2002
Days to Decision
124 days
Submission Type
Summary

HOMMED SENTRY III PATIENT MONITOR SYSTEM WITH CARD READER

Page Type
Cleared 510(K)
510(k) Number
K014025
510(k) Type
Traditional
Applicant
HOMMED LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/9/2002
Days to Decision
124 days
Submission Type
Summary