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HOMMED SENTRY III PATIENT MONITOR SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K004044
510(k) Type
Traditional
Applicant
HOMMED LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/2/2001
Days to Decision
63 days
Submission Type
Summary

HOMMED SENTRY III PATIENT MONITOR SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K004044
510(k) Type
Traditional
Applicant
HOMMED LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/2/2001
Days to Decision
63 days
Submission Type
Summary