The following data is part of a premarket notification filed by Vital Signs, Inc. with the FDA for Code Blue Manual Resuscitator.
Device ID | K831885 |
510k Number | K831885 |
Device Name: | CODE BLUE MANUAL RESUSCITATOR |
Classification | Ventilator, Emergency, Manual (resuscitator) |
Applicant | VITAL SIGNS, INC. 1 MADISON ST. East Rutherford, NJ 07073 |
Contact | Terence D Wall |
Correspondent | Terence D Wall VITAL SIGNS, INC. 1 MADISON ST. East Rutherford, NJ 07073 |
Product Code | BTM |
CFR Regulation Number | 868.5915 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1983-06-13 |
Decision Date | 1983-09-08 |