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FDA 510(k)

GEOFORM ANNULOPLASTY RING, MITRAL MODEL 4200

K-Number: K032250 · 2003-08-26

ApplicantEdwards Lifesciences, LLC
Decision Date2003-08-26
Product CodeKRH
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

GEOFORM ANNULOPLASTY RING, MITRAL MODEL 4200 is the device name listed in this FDA 510(k) record. The listed applicant is Edwards Lifesciences, LLC. It received FDA 510(k) clearance on 2003-08-26 under 510(k) number K032250. The device is classified under product code KRH. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GEOFORM ANNULOPLASTY RING, MITRAL MODEL 4200?

GEOFORM ANNULOPLASTY RING, MITRAL MODEL 4200 is a medical device that received FDA 510(k) clearance on 2003-08-26. The listed applicant is Edwards Lifesciences, LLC. The 510(k) number is K032250.

When did GEOFORM ANNULOPLASTY RING, MITRAL MODEL 4200 receive FDA 510(k) clearance?

GEOFORM ANNULOPLASTY RING, MITRAL MODEL 4200 received FDA 510(k) clearance on 2003-08-26, under 510(k) number K032250.

Who is the listed applicant for GEOFORM ANNULOPLASTY RING, MITRAL MODEL 4200?

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

What is the FDA product code for GEOFORM ANNULOPLASTY RING, MITRAL MODEL 4200?

The FDA product code for GEOFORM ANNULOPLASTY RING, MITRAL MODEL 4200 is KRH.

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Other records listing Edwards Lifesciences, LLC 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.

K251326Respiration Rate algorithmK253186HemoSphere Nano Monitor (HSNANO1)K251982Edwards MC3 Tricuspid annuloplasty ring (4900)K251688Carpentier-Edwards Physio Annuloplasty Ring (4450)K242518Hypertension Prediction Index (HePI) AlgorithmK242909FloTrac sensors; FloTrac Jr sensors; Acumen IQ sensors; VolumeView sensors

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Related Devices (Code: KRH)

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.

K261707MEMO 4D Curve™ Semirigid mitral annuloplasty ringCorcym S.r.l.K260498TriMemo™ SEMIRIGID ANNULOPLASTY RINGCorcym S.r.l.K253232Seguin Annuloplasty RingABBOTT MEDICALK251982Edwards MC3 Tricuspid annuloplasty ring (4900)Edwards Lifesciences, LLCK251688Carpentier-Edwards Physio Annuloplasty Ring (4450)Edwards Lifesciences, LLCK250859TransForm McCarthy Mitral Annuloplasty Ring (TF)Genesee Biomedical, 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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