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FDA 510(k)

NEOZOLINE VENTILATION TUBES

K-Number: K061058 · 2006-07-12

ApplicantAdept Medical, Ltd.
Decision Date2006-07-12
Product CodeETD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

NEOZOLINE VENTILATION TUBES is the device name listed in this FDA 510(k) record. The listed applicant is Adept Medical, Ltd.. It received FDA 510(k) clearance on 2006-07-12 under 510(k) number K061058. 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 NEOZOLINE VENTILATION TUBES?

NEOZOLINE VENTILATION TUBES is a medical device that received FDA 510(k) clearance on 2006-07-12. The listed applicant is Adept Medical, Ltd.. The 510(k) number is K061058.

When did NEOZOLINE VENTILATION TUBES receive FDA 510(k) clearance?

NEOZOLINE VENTILATION TUBES received FDA 510(k) clearance on 2006-07-12, under 510(k) number K061058.

Who is the listed applicant for NEOZOLINE VENTILATION TUBES?

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

What is the FDA product code for NEOZOLINE VENTILATION TUBES?

The FDA product code for NEOZOLINE VENTILATION TUBES is ETD.

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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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