510(k) K042253
K042253 is an FDA 510(k) premarket notification submitted by S.L.P. , Ltd. for the device "SLEEPSENSE SLEEP SENSORS". The FDA issued a decision of Substantially Equivalent on October 6, 2004. The device falls under product code MNR (Ventilatory Effort Recorder), a Class II device regulated under 21 CFR 868.2375. S.L.P. , Ltd. has at least 4 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 6, 2004
- Date Received
- August 20, 2004
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- Yes
Device Classification
- Device Name
- Ventilatory Effort Recorder
- Device Class
- Class II
- Regulation Number
- 868.2375
- Review Panel
- AN
- Submission Type