510(k) K140707
K140707 is an FDA 510(k) premarket notification submitted by International Biomedical for the device "LIFEBORNE INFANT RESUSCITATOR". The FDA issued a decision of Substantially Equivalent on May 28, 2014. The device falls under product code BTL (Ventilator, Emergency, Powered (Resuscitator)), a Class II device regulated under 21 CFR 868.5925. International Biomedical has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 28, 2014
- Date Received
- March 20, 2014
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Ventilator, Emergency, Powered (Resuscitator)
- Device Class
- Class II
- Regulation Number
- 868.5925
- Review Panel
- AN
- Submission Type