The following data is part of a premarket notification filed by Exmoor Plastics Ltd. with the FDA for Titanium Ventilation Tubes.
Device ID | K921923 |
510k Number | K921923 |
Device Name: | TITANIUM VENTILATION TUBES |
Classification | Tube, Tympanostomy |
Applicant | EXMOOR PLASTICS LTD. LISIEUX WAY Taunton, Somerset, GB Ta1 2lb |
Contact | Brian East |
Correspondent | Brian 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 | 1992-04-08 |
Decision Date | 1993-02-12 |