Care Cycle Connect Application— 510(k) K161411
Substantially EquivalentRespironics, Inc.
FDA 510(k) clearance K161411 for Care Cycle Connect Application, Substantially Equivalent on 2017-02-17. Applicant: Respironics, Inc.. Device class: 2.
Clearance details
- Applicant
- Respironics, Inc.
- Product code
- Code MOD
- Device class
- Class 2
- Regulation
- 21 CFR 868.5895
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Murrysville, PA, US
Recent devices under product code MOD
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