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FDA 510(k)

CO2 FIBEROPTIC DELIVERY SYSTEM/BRONCHOSCOPIC USE

K-Number: K862835 · 1987-02-05

ApplicantCooper Lasersonics, Inc.
Decision Date1987-02-05
Product CodeEOQ
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

CO2 FIBEROPTIC DELIVERY SYSTEM/BRONCHOSCOPIC USE is the device name listed in this FDA 510(k) record. The listed applicant is Cooper Lasersonics, Inc.. It received FDA 510(k) clearance on 1987-02-05 under 510(k) number K862835. 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 CO2 FIBEROPTIC DELIVERY SYSTEM/BRONCHOSCOPIC USE?

CO2 FIBEROPTIC DELIVERY SYSTEM/BRONCHOSCOPIC USE is a medical device that received FDA 510(k) clearance on 1987-02-05. The listed applicant is Cooper Lasersonics, Inc.. The 510(k) number is K862835.

When did CO2 FIBEROPTIC DELIVERY SYSTEM/BRONCHOSCOPIC USE receive FDA 510(k) clearance?

CO2 FIBEROPTIC DELIVERY SYSTEM/BRONCHOSCOPIC USE received FDA 510(k) clearance on 1987-02-05, under 510(k) number K862835.

Who is the listed applicant for CO2 FIBEROPTIC DELIVERY SYSTEM/BRONCHOSCOPIC USE?

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

What is the FDA product code for CO2 FIBEROPTIC DELIVERY SYSTEM/BRONCHOSCOPIC USE?

The FDA product code for CO2 FIBEROPTIC DELIVERY SYSTEM/BRONCHOSCOPIC USE is EOQ.

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Other records listing Cooper Lasersonics, 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.

K880808ILLUMINA MODEL 40 CO2 LASER FOR GENERAL/PLASTIC SUK880807ILLUMINA MODEL 25 CO2 LASER FOR GENERAL/PLASTIC SUK880427ILLUMINA 40 CO2 LASER SYSTEMK880428ILLUMINA 25 CO2 LASER SYSTEMK880429ILLUMINA 55 CO2 LASER SYSTEMK880809ILLUMINA MODEL 55 CO2 LASER FOR GENERAL/PLASTIC SU

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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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