The following data is part of a premarket notification filed by Custom Pack Reliability with the FDA for Cpr Yankauer.
| Device ID | K960223 |
| 510k Number | K960223 |
| Device Name: | CPR YANKAUER |
| Classification | Apparatus, Suction, Operating-room, Wall Vacuum Powered |
| Applicant | CUSTOM PACK RELIABILITY 4207 VINELAND ROAD, M-1 Orlando, FL 32811 |
| Contact | Richard L Ellwood |
| Correspondent | Richard L Ellwood CUSTOM PACK RELIABILITY 4207 VINELAND ROAD, M-1 Orlando, FL 32811 |
| Product Code | GCX |
| CFR Regulation Number | 880.6740 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-01-16 |
| Decision Date | 1996-03-28 |