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FDA 510(k)

FLEX FINDER GUIDEWIRE

K-Number: K923755 · 1993-09-03

ApplicantFlex Medics Corporation
Decision Date1993-09-03
Product CodeOCY
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

FLEX FINDER GUIDEWIRE is the device name listed in this FDA 510(k) record. The listed applicant is Flex Medics Corporation. It received FDA 510(k) clearance on 1993-09-03 under 510(k) number K923755. The device is classified under product code OCY. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLEX FINDER GUIDEWIRE?

FLEX FINDER GUIDEWIRE is a medical device that received FDA 510(k) clearance on 1993-09-03. The listed applicant is Flex Medics Corporation. The 510(k) number is K923755.

When did FLEX FINDER GUIDEWIRE receive FDA 510(k) clearance?

FLEX FINDER GUIDEWIRE received FDA 510(k) clearance on 1993-09-03, under 510(k) number K923755.

Who is the listed applicant for FLEX FINDER GUIDEWIRE?

The FDA 510(k) record lists Flex Medics Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FLEX FINDER GUIDEWIRE?

The FDA product code for FLEX FINDER GUIDEWIRE is OCY.

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Related Devices (Code: OCY)

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.

K153264EasyPass GuidewireMedi-Globe CorporationK131072ORCHESTRA HYDROPHILIC GUIDEWIRE STANDARD ANGLED, ORCHESTRA HYDROPHILIC GUIDEWIRE STRAIGHT STIFF, ORCHESTRA HYDROPHILICColoplast A/SK124052OSTAVI HYDROPHILIC GUIDEWIRELake Region MedicalK123438XENX STONE MANAGEMENT DEVICEXenolith MedicalK123439NEO ERCP GUIDEWIRENeometrics, Inc.K122816AXCESS SOFT TIP WIRE GUIDEWilson-Cook Medical, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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