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FDA 510(k)

ENK FIBEROPTIC ATOMIZER SET

K-Number: K031966 · 2003-10-16

ApplicantCook, Inc.
Decision Date2003-10-16
Product CodeEOQ
Advisory CommitteeEN
DecisionUnknown

Device Summary

ENK FIBEROPTIC ATOMIZER SET is the device name listed in this FDA 510(k) record. The listed applicant is Cook, Inc.. It received FDA 510(k) clearance on 2003-10-16 under 510(k) number K031966. The device is classified under product code EOQ. It was reviewed by the EN advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the ENK FIBEROPTIC ATOMIZER SET?

ENK FIBEROPTIC ATOMIZER SET is a medical device that received FDA 510(k) clearance on 2003-10-16. The listed applicant is Cook, Inc.. The 510(k) number is K031966.

When did ENK FIBEROPTIC ATOMIZER SET receive FDA 510(k) clearance?

ENK FIBEROPTIC ATOMIZER SET received FDA 510(k) clearance on 2003-10-16, under 510(k) number K031966.

Who is the listed applicant for ENK FIBEROPTIC ATOMIZER SET?

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

What is the FDA product code for ENK FIBEROPTIC ATOMIZER SET?

The FDA product code for ENK FIBEROPTIC ATOMIZER SET is EOQ.

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Other records listing Cook, Inc. as applicant

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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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