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

Page Type
Cleared 510(K)
PDF
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
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