The following data is part of a premarket notification filed by Engineered Medical Systems with the FDA for Pressure Limiting Elbow.
Device ID | K932797 |
510k Number | K932797 |
Device Name: | PRESSURE LIMITING ELBOW |
Classification | Ventilator, Emergency, Manual (resuscitator) |
Applicant | ENGINEERED MEDICAL SYSTEMS 8529 ZIONSVILLE RD. P.O. BOX 681514 Indianapolis, IN 46268 |
Contact | Jeff Quinn |
Correspondent | Jeff Quinn ENGINEERED MEDICAL SYSTEMS 8529 ZIONSVILLE RD. P.O. BOX 681514 Indianapolis, IN 46268 |
Product Code | BTM |
CFR Regulation Number | 868.5915 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-06-09 |
Decision Date | 1993-09-03 |