The following data is part of a premarket notification filed by Exmoor Plastics Ltd. with the FDA for 'exmoor' Cawood Nasal Splints.
Device ID | K864932 |
510k Number | K864932 |
Device Name: | 'EXMOOR' CAWOOD NASAL SPLINTS |
Classification | Splint, Nasal |
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 | EPP |
CFR Regulation Number | 874.5800 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-12-16 |
Decision Date | 1987-03-04 |