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FDA 510(k)

RICHARD ROD LENS LARYNGOSCOPE

K-Number: K941264 · 1994-07-18

ApplicantSmith & Nephew Richards, Inc.
Decision Date1994-07-18
Product CodeEOQ
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

RICHARD ROD LENS LARYNGOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew Richards, Inc.. It received FDA 510(k) clearance on 1994-07-18 under 510(k) number K941264. The device is classified under product code EOQ. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RICHARD ROD LENS LARYNGOSCOPE?

RICHARD ROD LENS LARYNGOSCOPE is a medical device that received FDA 510(k) clearance on 1994-07-18. The listed applicant is Smith & Nephew Richards, Inc.. The 510(k) number is K941264.

When did RICHARD ROD LENS LARYNGOSCOPE receive FDA 510(k) clearance?

RICHARD ROD LENS LARYNGOSCOPE received FDA 510(k) clearance on 1994-07-18, under 510(k) number K941264.

Who is the listed applicant for RICHARD ROD LENS LARYNGOSCOPE?

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

What is the FDA product code for RICHARD ROD LENS LARYNGOSCOPE?

The FDA product code for RICHARD ROD LENS LARYNGOSCOPE is EOQ.

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Other records listing Smith & Nephew Richards, 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.

K965224EMPOWER ANTERIOR DIRECT SCREWSK963509GLOBAL TAPER TAPERED HIP SYSTEM, GT SPECTRONK960444FINN ROD TO ROD CONNECTORK964163TRIMAX NAIL SYSTEMK962557GENESIS II ZIRCONIUM FEMORAL COMPONENT/PROFIX ZIRCONIUM FEMORAL COMPONENTK963486REVISION HIP SYSTEM

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Related Devices (Code: EOQ)

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.

K261637Single-use Flexible BronchoscopeHunan Vathin Medical Instrument Co., Ltd.K260309Ambu® aScope™ 5 Broncho 2.7/1.2; Ambu® aScope™ 5 Broncho 4.2/2.2; Ambu® aScope™ 5 Broncho 4.2/2.2 Sampler SetAmbu A/SK2540263.8mm Slim ProVu Video Bronchoscope (090-02-0038U); 5.0mm Regular ProVu Video Bronchoscope (090-02-0050U); 6.0mm Large ProVu Video Bronchoscope (090-02-0060U); ProVu Video Bronchoscope 8 display (040-07-0082U)Flexicare Medical Limited.K260382MONARCH™ Platform (MON-000008)Auris Health, Inc.K254037LungFlow Airway CatheterFree Flow Medical, Inc.K253137FUJIFILM Endoscope Model EB-840S; FUJIFILM Endoscope Model EB-840TFujifilm Corporation

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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