Last synced on 2 December 2022 at 11:04 pm

RESPITRACE PLUS, RESPIBANDS, AND RESPICENTRAL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K903011
510(k) Type
Traditional
Applicant
NON-INVASIVE MONITORING SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/29/1991
Days to Decision
263 days

RESPITRACE PLUS, RESPIBANDS, AND RESPICENTRAL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K903011
510(k) Type
Traditional
Applicant
NON-INVASIVE MONITORING SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/29/1991
Days to Decision
263 days