FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
Masimo Rad-97 and Accessories
K Number: K170168
·
Decision Sep 14, 2017
Classifications
1
FEI Numbers
177
Registration Numbers
177
Same Product Code
305
Applicant Total
85
Review Days
238
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Basic Information
- Device Name
- Masimo Rad-97 and Accessories
- K Number
- K170168
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.2300
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Masimo Corporation
- Date Received
- January 19, 2017
- Decision Date
- September 14, 2017
- Product Code
- MWI
- Advisory Committee
- Cardiovascular
- Review Advisory Committee
- CV
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| MWI | Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms) | FDA class 2 | Cardiovascular |
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| K250757 | Radius VSM and Accessories | May 29, 2025 | Substantially Equivalent |
| K243305 | Masimo W1 | Apr 3, 2025 | Substantially Equivalent |
| K240229 | Masimo W1 | Aug 8, 2024 | Substantially Equivalent |
| K234021 | Masimo Stork | May 3, 2024 | Substantially Equivalent |
| K214115 | MightySat -OTC | Jan 31, 2024 | Substantially Equivalent |
| K223721 | Masimo Stork | Dec 15, 2023 | Substantially Equivalent |
| K232512 | Masimo W1 | Nov 17, 2023 | Substantially Equivalent |
| DEN200076 | ORi | Oct 12, 2023 | Unknown |