Last synced on 4 February 2023 at 10:33 pm

OPTOVENT RESPIRATORY MONITOR MODEL NUMBER RR 9700

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981725
510(k) Type
Traditional
Applicant
OPTOVENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/2/1999
Days to Decision
263 days
Submission Type
Statement

OPTOVENT RESPIRATORY MONITOR MODEL NUMBER RR 9700

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981725
510(k) Type
Traditional
Applicant
OPTOVENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/2/1999
Days to Decision
263 days
Submission Type
Statement