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FDA 510(k)

DISPOSABLE BENDING CANNULA PR-233Q

K-Number: K011149 · 2001-05-15

ApplicantThe Olympus Optical Co.
Decision Date2001-05-15
Product CodeODD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE BENDING CANNULA PR-233Q 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 2001-05-15 under 510(k) number K011149. The device is classified under product code ODD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE BENDING CANNULA PR-233Q?

DISPOSABLE BENDING CANNULA PR-233Q is a medical device that received FDA 510(k) clearance on 2001-05-15. The listed applicant is The Olympus Optical Co.. The 510(k) number is K011149.

When did DISPOSABLE BENDING CANNULA PR-233Q receive FDA 510(k) clearance?

DISPOSABLE BENDING CANNULA PR-233Q received FDA 510(k) clearance on 2001-05-15, under 510(k) number K011149.

Who is the listed applicant for DISPOSABLE BENDING CANNULA PR-233Q?

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 DISPOSABLE BENDING CANNULA PR-233Q?

The FDA product code for DISPOSABLE BENDING CANNULA PR-233Q is ODD.

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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: ODD)

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.

K250573Single Use Cannula V PR-V223Q/V414Q/V416Q/V418Q/V420Q/V427Q/V434Q/V435Q; Single Use 2-Lumen Cannula V PR-V614MOlympus Medical Systems Corp.K202583BioShield biopsy valve EUS - LinearSTERIS CorporationK171989Classic ERCP Catheter and Huibregtse-Katon ERCP Catheter and Huibregtse-Katon Angled, Glo-Tip ERCP Catheter, Glo-Tip II Double Lumen ERCP Catheter & w/ Radiopaque Bands, Fusion ERCP Catheter with DomeTip and Fusion OMNI ERCP Catheter with DomeTip, Haber RAMP Catheter, Soehendra Universal CatheterWilson-Cook Medical, Inc.K070420BIOSHIELD-ERCP BIOPSY VALVE, MODEL 00711138United States Endoscopy Group, Inc.K010993ALIEN RX MICRO CANNULA, MODEL 4530Boston Scientific CorpK973205WILSON-COOK STRICTURE MEASURING CATHETERWilson-Cook Medical, Inc.

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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