The following data is part of a premarket notification filed by Exmoor Plastics Ltd. with the FDA for Sunderland Nasal Tube.
| Device ID | K883668 |
| 510k Number | K883668 |
| Device Name: | SUNDERLAND NASAL TUBE |
| Classification | Airway, Nasopharyngeal |
| Applicant | EXMOOR PLASTICS LTD. LISIEUX WAY Taunton, Somerset, GB Ta1 2lb |
| Contact | Brian G East |
| Correspondent | Brian G East EXMOOR PLASTICS LTD. LISIEUX WAY Taunton, Somerset, GB Ta1 2lb |
| Product Code | BTQ |
| CFR Regulation Number | 868.5100 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-08-26 |
| Decision Date | 1988-11-21 |