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RESPIEVENTS, VERSION 4.2

Page Type
Cleared 510(K)
510(k) Number
K001369
510(k) Type
Traditional
Applicant
Non-Invasive Monitoring Systems, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/26/2000
Days to Decision
86 days
Submission Type
Summary

RESPIEVENTS, VERSION 4.2

Page Type
Cleared 510(K)
510(k) Number
K001369
510(k) Type
Traditional
Applicant
Non-Invasive Monitoring Systems, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/26/2000
Days to Decision
86 days
Submission Type
Summary