Last synced on 1 July 2022 at 11:04 pm

RESPITRAK

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K884959
510(k) Type
Traditional
Applicant
NON-INVASIVE MONITORING SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/8/1989
Days to Decision
191 days

RESPITRAK

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K884959
510(k) Type
Traditional
Applicant
NON-INVASIVE MONITORING SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/8/1989
Days to Decision
191 days