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FDA 510(k)

LUXTEC, KILLIAN AND VIENNA NASAL SPECULUMS

K-Number: K864383 · 1987-01-14

ApplicantLuxtec Corp.
Decision Date1987-01-14
Product CodeEQH
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

LUXTEC, KILLIAN AND VIENNA NASAL SPECULUMS is the device name listed in this FDA 510(k) record. The listed applicant is Luxtec Corp.. It received FDA 510(k) clearance on 1987-01-14 under 510(k) number K864383. The device is classified under product code EQH. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LUXTEC, KILLIAN AND VIENNA NASAL SPECULUMS?

LUXTEC, KILLIAN AND VIENNA NASAL SPECULUMS is a medical device that received FDA 510(k) clearance on 1987-01-14. The listed applicant is Luxtec Corp.. The 510(k) number is K864383.

When did LUXTEC, KILLIAN AND VIENNA NASAL SPECULUMS receive FDA 510(k) clearance?

LUXTEC, KILLIAN AND VIENNA NASAL SPECULUMS received FDA 510(k) clearance on 1987-01-14, under 510(k) number K864383.

Who is the listed applicant for LUXTEC, KILLIAN AND VIENNA NASAL SPECULUMS?

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

What is the FDA product code for LUXTEC, KILLIAN AND VIENNA NASAL SPECULUMS?

The FDA product code for LUXTEC, KILLIAN AND VIENNA NASAL SPECULUMS is EQH.

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Other records listing Luxtec Corp. 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.

K973193LUXSCOPEK970642TENOSCOPEK970562TENOSNAREK950960REDDY ILLUMINATORK895248IMS5000 ILLUMINATED LOUPESK890716LUXTEC ACO SERIES 4000 LIGHT SOURCE

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Related Devices (Code: EQH)

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.

K945876WECO ENDOSCOPIC SYSTEM WITH FIBER OPTIC LIGHTWells Johnson Co.K954184JED-LIGHT FIBEROPTIC LIGHT SOURCEJedmed Instrument Co.K951829COLD LIGHT SOURCE LOS 150Laser-Optik-Systeme GmbH & Co. KGK932771BATTERY POWERED, DISPOSABLE ENDOSCOPE LIGHT SOURCEXomed-Treace, Inc.K941661GM OPTI*CAM CAMER WITH DENTAL FIBER OPTIC LIGHTGm Engineering, Inc.K941662GM OPTI*CAM CAMERA WITH ENT FIBER OPTIC LIGHTGm Engineering, 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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