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FDA 510(k)

EXMOOR AURAL GROMMET AG/T4

K-Number: K810705 · 1981-04-14

ApplicantExmoor Plastics , Ltd.
Decision Date1981-04-14
Product CodeETD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

EXMOOR AURAL GROMMET AG/T4 is the device name listed in this FDA 510(k) record. The listed applicant is Exmoor Plastics , Ltd.. It received FDA 510(k) clearance on 1981-04-14 under 510(k) number K810705. The device is classified under product code ETD. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EXMOOR AURAL GROMMET AG/T4?

EXMOOR AURAL GROMMET AG/T4 is a medical device that received FDA 510(k) clearance on 1981-04-14. The listed applicant is Exmoor Plastics , Ltd.. The 510(k) number is K810705.

When did EXMOOR AURAL GROMMET AG/T4 receive FDA 510(k) clearance?

EXMOOR AURAL GROMMET AG/T4 received FDA 510(k) clearance on 1981-04-14, under 510(k) number K810705.

Who is the listed applicant for EXMOOR AURAL GROMMET AG/T4?

The FDA 510(k) record lists Exmoor Plastics , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EXMOOR AURAL GROMMET AG/T4?

The FDA product code for EXMOOR AURAL GROMMET AG/T4 is ETD.

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Other records listing Exmoor Plastics , Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K093863EPIDRUMK990366EXMOOR SUCTION CLEARANCE KITK980828EXMOOR MYRINGOTOMY KITK981143DILKES LASER/SUCTION CANNULAEK972700EXMOOR ATTIC AND MASTOID ANTRUM MIDDLE EAR IMPLANT (EMMETT CAMPBELL MD FACS PATTERN)K981088MILLS COLUMELLA PROSTHESIS

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Related Devices (Code: ETD)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K252436Tula Tympanostomy Tube Delivery DeviceTusker Medical, Inc.K250256Solo+ Tympanostomy Tube Device (TTD), Solo+ TTD, Solo+ (Solo+ Tympanostomy Tube Handpiece (Catalogue #: 12115-100-000) and Solo+ Tympanostomy Tube Cartridge (Catalogue #: 12115-200-000))Aventamed DacK232702Solo+ Tympanostomy Tube Device (TTD)Aventamed DacK233658Biowy Tym Tube (TT)Biowy CorporationK232059Tympanostomy TubesGrace Medical, Inc.K221254Hummingbird Tympanostomy Tube SystemPreceptis Medical, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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