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FDA 510(k)

OLYMPUS SPRAY CATHETER PW-6C-1

K-Number: K012073 · 2001-08-10

ApplicantThe Olympus Optical Co.
Decision Date2001-08-10
Product CodeEOQ
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

OLYMPUS SPRAY CATHETER PW-6C-1 is the device name listed in this FDA 510(k) record. The listed applicant is The Olympus Optical Co.. It received FDA 510(k) clearance on 2001-08-10 under 510(k) number K012073. 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 OLYMPUS SPRAY CATHETER PW-6C-1?

OLYMPUS SPRAY CATHETER PW-6C-1 is a medical device that received FDA 510(k) clearance on 2001-08-10. The listed applicant is The Olympus Optical Co.. The 510(k) number is K012073.

When did OLYMPUS SPRAY CATHETER PW-6C-1 receive FDA 510(k) clearance?

OLYMPUS SPRAY CATHETER PW-6C-1 received FDA 510(k) clearance on 2001-08-10, under 510(k) number K012073.

Who is the listed applicant for OLYMPUS SPRAY CATHETER PW-6C-1?

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

What is the FDA product code for OLYMPUS SPRAY CATHETER PW-6C-1?

The FDA product code for OLYMPUS SPRAY CATHETER PW-6C-1 is EOQ.

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Other records listing The Olympus Optical Co. 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.

K032066SONOSURG SYSTEMK030194XUES-41 ENDOSCOPIC ELECTROSURGICAL UNITK021962OLYMPUS ULTRASONIC SURGICAL SYSTEMK023984MODIFICATION TO OLYMPUS BRONCHOSCOPES BF-40 SERIES, BF-240 SERIES, AND BF-160 SERIESK023272DISPOSABLE ASPIRATION NEEDLE NA-200HK023767UES-30 ELECTROSURGICAL UNIT AND IT'S ASSOCIATED ACCESSORIES

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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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