510(k) K921431
K921431 is an FDA 510(k) premarket notification submitted by Ideas For Living for the device "POTTY PAGER". The FDA issued a decision of Substantially Equivalent on July 21, 1992. The device falls under product code KPN (Alarm, Conditioned Response Enuresis), a Class II device regulated under 21 CFR 876.2040.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 21, 1992
- Date Received
- March 25, 1992
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Alarm, Conditioned Response Enuresis
- Device Class
- Class II
- Regulation Number
- 876.2040
- Review Panel
- GU
- Submission Type