'EXMOOR' T-TUBE

Tube, Tympanostomy

EXMOOR PLASTICS LTD.

The following data is part of a premarket notification filed by Exmoor Plastics Ltd. with the FDA for 'exmoor' T-tube.

Pre-market Notification Details

Device IDK871035
510k NumberK871035
Device Name:'EXMOOR' T-TUBE
ClassificationTube, Tympanostomy
Applicant EXMOOR PLASTICS LTD. LISIEUX WAY Taunton, Somerset,  GB Ta1 2lb
ContactBrian G East
CorrespondentBrian G East
EXMOOR PLASTICS LTD. LISIEUX WAY Taunton, Somerset,  GB Ta1 2lb
Product CodeETD  
CFR Regulation Number874.3880 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1987-03-17
Decision Date1987-03-23

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