Medline ReNewal Reprocessed Nellcor OxiMax SpO2 Sensor— 510(k) K201699
Substantially EquivalentSurgical Instrument and Savings Inc (Dba Medline Renewal)
FDA 510(k) clearance K201699 for Medline ReNewal Reprocessed Nellcor OxiMax SpO2 Sensor, Substantially Equivalent on 2020-07-22. Applicant: Surgical Instrument and Savings Inc (Dba Medline Renewal). Device class: 2.
Clearance details
- Applicant
- Surgical Instrument and Savings Inc (Dba Medline Renewal)
- Product code
- Code NLF
- Device class
- Class 2
- Regulation
- 21 CFR 870.2700
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Redmond, OR, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.