The following data is part of a premarket notification filed by Ambu, Inc. with the FDA for Spur Adult With Open Reservoir System.
Device ID | K922707 |
510k Number | K922707 |
Device Name: | SPUR ADULT WITH OPEN RESERVOIR SYSTEM |
Classification | Ventilator, Emergency, Manual (resuscitator) |
Applicant | AMBU, INC. 611 NORTH HAMMONDS FERRY RD. Linthicum, MD 21090 -1356 |
Contact | David Lee |
Correspondent | David Lee AMBU, INC. 611 NORTH HAMMONDS FERRY RD. Linthicum, MD 21090 -1356 |
Product Code | BTM |
CFR Regulation Number | 868.5915 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-06-05 |
Decision Date | 1992-06-19 |