The following data is part of a premarket notification filed by Exmoor Plastics Ltd. with the FDA for 'exmoor' T-tube.
Device ID | K871035 |
510k Number | K871035 |
Device Name: | 'EXMOOR' T-TUBE |
Classification | Tube, Tympanostomy |
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 | ETD |
CFR Regulation Number | 874.3880 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-03-17 |
Decision Date | 1987-03-23 |