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FDA 510(k)

XOMED PLATINUM WIRE TEFLON PISTION

K-Number: K872112 · 1987-07-02

ApplicantXomed, Inc.
Decision Date1987-07-02
Product CodeETB
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

XOMED PLATINUM WIRE TEFLON PISTION is the device name listed in this FDA 510(k) record. The listed applicant is Xomed, Inc.. It received FDA 510(k) clearance on 1987-07-02 under 510(k) number K872112. The device is classified under product code ETB. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the XOMED PLATINUM WIRE TEFLON PISTION?

XOMED PLATINUM WIRE TEFLON PISTION is a medical device that received FDA 510(k) clearance on 1987-07-02. The listed applicant is Xomed, Inc.. The 510(k) number is K872112.

When did XOMED PLATINUM WIRE TEFLON PISTION receive FDA 510(k) clearance?

XOMED PLATINUM WIRE TEFLON PISTION received FDA 510(k) clearance on 1987-07-02, under 510(k) number K872112.

Who is the listed applicant for XOMED PLATINUM WIRE TEFLON PISTION?

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

What is the FDA product code for XOMED PLATINUM WIRE TEFLON PISTION?

The FDA product code for XOMED PLATINUM WIRE TEFLON PISTION is ETB.

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Other records listing Xomed, Inc. 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.

K002395MODEL 30 CLASSIC PNEUMATONOMETERK002987REDTRONIC XOMED MONOPOLAR ENERGIZED BLADEK002828XPS NITRO SYSTEMK002897TITANIUM MIDDLE EAR PROSTHESESK993653MICRO-FRANCE TROCARS AND ACCESSORIESK001148MEROGEL OTOLOGIC PACK

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Related Devices (Code: ETB)

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.

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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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