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FDA 510(k)

FLEXFINDER GUIDEWIRE

K-Number: K942074 · 1994-06-24

ApplicantFlexmedics
Decision Date1994-06-24
Product CodeKNY
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

FLEXFINDER GUIDEWIRE is the device name listed in this FDA 510(k) record. The listed applicant is Flexmedics. It received FDA 510(k) clearance on 1994-06-24 under 510(k) number K942074. The device is classified under product code KNY. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLEXFINDER GUIDEWIRE?

FLEXFINDER GUIDEWIRE is a medical device that received FDA 510(k) clearance on 1994-06-24. The listed applicant is Flexmedics. The 510(k) number is K942074.

When did FLEXFINDER GUIDEWIRE receive FDA 510(k) clearance?

FLEXFINDER GUIDEWIRE received FDA 510(k) clearance on 1994-06-24, under 510(k) number K942074.

Who is the listed applicant for FLEXFINDER GUIDEWIRE?

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

What is the FDA product code for FLEXFINDER GUIDEWIRE?

The FDA product code for FLEXFINDER GUIDEWIRE is KNY.

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Other records listing Flexmedics 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.

K990765FLEXFINDER GUIDE WIRE(REGULAR SHAFT/STIFF SHAFT) MARKED INK BANDS, FLEXFINDER GUIDE WIRE (REGULAR SHAFT/STIFF SHAFT) NOK964955FLEXFINDER GUIDEWIRE (REGULAR SHAFT/STIFF SHAFT) MARKED INK BANDS ENCAP+/GUIDEWIRE(REGULAR SHAFT/STIFF SHAFT) NO MARKINGK952430FINESSE GUIDEWIRE CORONARYK943390FLEXFINDER GUIDEWIREK934265FLEXMEDICS SUPER-SEVEN STRANDED NICKEL-TITANIUM ARCHWIREK912843FLEXMEDICS RETRACT ORTH PROBE, PETTINE BONE PROBE

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Related Devices (Code: KNY)

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.

K260919Transurethral Catheter Safety Valve (TUCSV) (80050)Class Medical , Ltd.K182144Bi-Flex EvoPromepla SamK162356Vesair Cystoscopic SheathSolace TherapeuticsK131803GUARDIAN URETHRAL SHEATHSolace TherapeuticsK123170VARI-PASS VARIABLE LENGTH ACCESS SHEATHOlympus Surgical Technologies AmericaK120160ROCAMED ROCAUS PLATINUMPromepla Sam

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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