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FDA 510(k), K812460, VARIOUS AURAL GROMMETS
FDA 510(k), K812460, VARIOUS AURAL GROMMETS
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510(K) Number: K812460
Device Name: VARIOUS AURAL GROMMETS
Manufacturer: EXMOOR PLASTICS LTD.
Device Classification Name: tube, tympanostomy
Regulation Number: 874.3880
Classification Product Code: ETD
Date Received: 08/31/1981
Decision Date: 09/21/1981
Regulation Medical Specialty: Ear Nose & Throat
Device Name: VARIOUS AURAL GROMMETS
Manufacturer: EXMOOR PLASTICS LTD.
Device Classification Name: tube, tympanostomy
Regulation Number: 874.3880
Classification Product Code: ETD
Date Received: 08/31/1981
Decision Date: 09/21/1981
Regulation Medical Specialty: Ear Nose & Throat
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- Delivery: Approximately 1 to 2 weeks
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