Data / Medical devices / United States / S.L.P. Inc.
S.L.P. Inc.: FDA-registered device maker in Elgin, IL, United States, 2 510(k) clearances
S.L.P. Inc. is registered with the FDA (registration 3006463573) in Elgin, IL, United States. It lists 3 device types. The FDA files 2 510(k) clearances under its listings, the newest dated October 7, 2010. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3006463573
- Address
- 2511 Technology Drive, Suite 112, Elgin, IL, United States, 60124
- Owner or operator
- S.L.P. INC. (9068058)
- Roles
- Repackager or relabeler
- First device listed
- December 11, 2011
- Registered through
- 2026
- Brand names listed
- Accessory to transducer gas pressure, SleepSense, sleepsense
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Oximeter | DQA | 2 | Repackager or relabeler | accessdata.fda.gov |
| Transducer, Gas Pressure | BXO | 1 | Repackager or relabeler | accessdata.fda.gov |
| Ventilatory Effort Recorder | MNR | 2 | Repackager or relabeler | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| October 7, 2010 | K100077 | NELLCOR COMPATIBLE REUSABLE SPO2 SOFT-FINGER SENSOR, MODEL T100A-090103 | DQA | Substantially Equivalent | Solaris Medical Technology, Inc. | accessdata.fda.gov |
| October 6, 2004 | K042253 | SLEEPSENSE SLEEP SENSORS | MNR | Substantially Equivalent | S.L.P. , Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Transducer, Gas Pressure
- All makers of Oximeter
- All makers of Ventilatory Effort Recorder
Updated October 7, 2010. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.