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FDA 510(k)

EB-1830T3, VIDEO BRONCHOSCOPE

K-Number: K023376 · 2002-10-16

ApplicantPentax Precision Instrument Corp.
Decision Date2002-10-16
Product CodeEOQ
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

EB-1830T3, VIDEO BRONCHOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Pentax Precision Instrument Corp.. It received FDA 510(k) clearance on 2002-10-16 under 510(k) number K023376. 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 EB-1830T3, VIDEO BRONCHOSCOPE?

EB-1830T3, VIDEO BRONCHOSCOPE is a medical device that received FDA 510(k) clearance on 2002-10-16. The listed applicant is Pentax Precision Instrument Corp.. The 510(k) number is K023376.

When did EB-1830T3, VIDEO BRONCHOSCOPE receive FDA 510(k) clearance?

EB-1830T3, VIDEO BRONCHOSCOPE received FDA 510(k) clearance on 2002-10-16, under 510(k) number K023376.

Who is the listed applicant for EB-1830T3, VIDEO BRONCHOSCOPE?

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

What is the FDA product code for EB-1830T3, VIDEO BRONCHOSCOPE?

The FDA product code for EB-1830T3, VIDEO BRONCHOSCOPE is EOQ.

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Other records listing Pentax Precision Instrument 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.

K041397EG-3830UTK041396FG-36UX FIBER ULTRASOUND GASTROSCOPEK041395EG-3630URK031789EG-3830UT, VIDEO ULTRASOUND GASTROSCOPEK023401EG-3830UT, VIDEO ULTRASOUND GASTROSCOPEK021276FG-36UX FIBER ULTRASOUND GASTROSCOPE

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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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