Reprocessed RD SET Adt Pulse Oximeter Sensor (4000), Reprocessed RD SET Pdt Pulse Oximeter Sensor (4001), Reprocessed RD SET Inf Pulse Oximeter Sensor (4002), Reprocessed RD SET Adt Pulse Oximeter Sensor (4003)
K222019 is the FDA 510(k) clearance record for Reprocessed RD SET Adt Pulse Oximeter Sensor (4000), Reprocessed RD SET Pdt Pulse Oximeter Sensor (4001), Reprocessed RD SET Inf Pulse Oximeter Sensor (4002), Reprocessed RD SET Adt Pulse Oximeter Sensor (4003), a class II device, cleared for Stryker Sustainability Solutions on under FDA product code NLF (Oximeter, Reprocessed). FDA's definition for product code NLF reads: "same as DQA except reprocessed. Reprocessing validation data for this device type must be included in a 510(k) submission. (70 FR 56911, available at https://www.govinfo.gov/content/pkg/FR-2005-09-29/pdf/05-19510.pdf)". FDA records list 88 510(k) clearances for Stryker Sustainability Solutions, from to . As of , FDA records show no recalls naming K222019.
Clearance record
- Decision date
- Received
- (149 days to decision)
- Product code
- NLF Oximeter, Reprocessed
- Regulation
- 21 CFR 870.2700
- Device class
- Class II
- Review panel
- Cardiovascular
- Applicant
- Stryker Sustainability Solutions 1810 W Dr.Ake Dr., Tempe AZ
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code NLF
Trailing 12 monthsFDA records hold no clearances under product code NLF in the trailing twelve months.
Show the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 0 |
| January 2026 | 0 |
| February 2026 | 0 |
| March 2026 | 0 |
| April 2026 | 0 |
| May 2026 | 0 |
| June 2026 | 0 |
| July 2026 | 0 |
| August 2026 | 0 |
| September 2026 | 0 |
| October 2026 | 0 |
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