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FDA 510(k)

ENDO FLIP

K-Number: K102214 · 2010-12-16

ApplicantCrospon, Ltd.
Decision Date2010-12-16
Product CodeFFX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ENDO FLIP is the device name listed in this FDA 510(k) record. The listed applicant is Crospon, Ltd.. It received FDA 510(k) clearance on 2010-12-16 under 510(k) number K102214. The device is classified under product code FFX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDO FLIP?

ENDO FLIP is a medical device that received FDA 510(k) clearance on 2010-12-16. The listed applicant is Crospon, Ltd.. The 510(k) number is K102214.

When did ENDO FLIP receive FDA 510(k) clearance?

ENDO FLIP received FDA 510(k) clearance on 2010-12-16, under 510(k) number K102214.

Who is the listed applicant for ENDO FLIP?

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

What is the FDA product code for ENDO FLIP?

The FDA product code for ENDO FLIP is FFX.

Other records listing Crospon, Ltd. 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.

K183072EndoFLIP SystemK172128EsoFLIP® ES-310 Balloon CatheterK170833EndoFLIP® System with FLIP Topography moduleK160725EndoFLIPK132337ESOFLIP BALLOON DILATION CATHETERK130906ENDOFLIP CATHETER

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Related Devices (Code: FFX)

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.

K252605mcompass Anorectal Balloon Expulsion Catheter (RMD-003-001)Medspira, LLCK240007Solar Compact (G4-1)Laborie Medical Technologies, Corp.K231861EndoflipTM 300 SystemCovidien, LLCK223705EndoflipTM 300Covidien, LLCK222000Transit-PelletsMedifactia ABK201106IntraMarX 3D Radiopaque MarkerAnx Robotica Corp

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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