510(k) K073171
K073171 is an FDA 510(k) premarket notification submitted by Allied Healthcare Products, Inc. for the device "RESUSCITATION TIMER, MODEL L770-CPR". The FDA issued a decision of Substantially Equivalent on January 31, 2008. The device falls under product code BTM (Ventilator, Emergency, Manual (Resuscitator)), a Class II device regulated under 21 CFR 868.5915. Allied Healthcare Products, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 31, 2008
- Date Received
- November 9, 2007
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Ventilator, Emergency, Manual (Resuscitator)
- Device Class
- Class II
- Regulation Number
- 868.5915
- Review Panel
- AN
- Submission Type