Last synced on 2 December 2022 at 11:04 pm

OPTOVENT RESPONS, OPTOVENT RENEE (OPTOVENT RESPONS WITHOUT PULSE OXIMETRY MODULE)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K003704
510(k) Type
Traditional
Applicant
OPTOVENT AB
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/5/2001
Days to Decision
66 days
Submission Type
Statement

OPTOVENT RESPONS, OPTOVENT RENEE (OPTOVENT RESPONS WITHOUT PULSE OXIMETRY MODULE)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K003704
510(k) Type
Traditional
Applicant
OPTOVENT AB
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/5/2001
Days to Decision
66 days
Submission Type
Statement