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FDA 510(k), K810701, EXMOOR AURAL GROMMET
FDA 510(k), K810701, EXMOOR AURAL GROMMET
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$149.00 USD
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$149.00 USD
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510(K) Number: K810701
Device Name: EXMOOR AURAL GROMMET
Manufacturer: EXMOOR PLASTICS LTD.
Device Classification Name: tube, tympanostomy
Regulation Number: 874.3880
Classification Product Code: ETD
Date Received: 03/16/1981
Decision Date: 04/14/1981
Regulation Medical Specialty: Ear Nose & Throat
Device Name: EXMOOR AURAL GROMMET
Manufacturer: EXMOOR PLASTICS LTD.
Device Classification Name: tube, tympanostomy
Regulation Number: 874.3880
Classification Product Code: ETD
Date Received: 03/16/1981
Decision Date: 04/14/1981
Regulation Medical Specialty: Ear Nose & Throat
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