Puritan Bennett Cuff Pressure Manager— 510(k) K202874
Substantially EquivalentCovidien, LLC
FDA 510(k) clearance K202874 for Puritan Bennett Cuff Pressure Manager, Substantially Equivalent on 2021-01-09. Applicant: Covidien, LLC. Device class: 2.
Clearance details
- Applicant
- Covidien, LLC
- Product code
- Code BSK
- Device class
- Class 2
- Regulation
- 21 CFR 868.5750
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Shanghai, CN
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Recalls naming K202874
K-number listed on FDA's recall recordMatched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K202874.
Data sourced from openFDA. This site is unofficial and independent of the FDA.