The following data is part of a premarket notification filed by Vital Signs, Inc. with the FDA for Resuscitation Circuit.
| Device ID | K812273 |
| 510k Number | K812273 |
| Device Name: | RESUSCITATION CIRCUIT |
| 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 | 1981-08-13 |
| Decision Date | 1981-08-25 |