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FDA 510(k)

RENU MEDICAL REPROCESSED ALP 1 CALF GARMENT, MODEL ALP1

K-Number: K051227 · 2006-04-07

ApplicantRenu Medical, Inc.
Decision Date2006-04-07
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

RENU MEDICAL REPROCESSED ALP 1 CALF GARMENT, MODEL ALP1 is the device name listed in this FDA 510(k) record. The listed applicant is Renu Medical, Inc.. It received FDA 510(k) clearance on 2006-04-07 under 510(k) number K051227. The device is classified under product code JOW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RENU MEDICAL REPROCESSED ALP 1 CALF GARMENT, MODEL ALP1?

RENU MEDICAL REPROCESSED ALP 1 CALF GARMENT, MODEL ALP1 is a medical device that received FDA 510(k) clearance on 2006-04-07. The listed applicant is Renu Medical, Inc.. The 510(k) number is K051227.

When did RENU MEDICAL REPROCESSED ALP 1 CALF GARMENT, MODEL ALP1 receive FDA 510(k) clearance?

RENU MEDICAL REPROCESSED ALP 1 CALF GARMENT, MODEL ALP1 received FDA 510(k) clearance on 2006-04-07, under 510(k) number K051227.

Who is the listed applicant for RENU MEDICAL REPROCESSED ALP 1 CALF GARMENT, MODEL ALP1?

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

What is the FDA product code for RENU MEDICAL REPROCESSED ALP 1 CALF GARMENT, MODEL ALP1?

The FDA product code for RENU MEDICAL REPROCESSED ALP 1 CALF GARMENT, MODEL ALP1 is JOW.

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Other records listing Renu Medical, Inc. as applicant

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K203847Reprocessed Tri Pulse Compression GarmentK121145RENU MEDICAL REPROCESSED AIRCAST VENAFLOW CALF GARMENTS/ALL SIZES, RENU MEDICAL REPROCESSED AIRCAST VENAFLOW THIGH GARMEK111773RENU MEDICAL REPROCESSED OXIMAX SENSORS: ADULT, PEDIATRIC, INFANT AND NEONATEK093658RENU MEDICAL VASOPRESS CALF , THIGH GARMENTS- ALL SIZESD, RENU MEDICAL VASOPRESS FOOT GARMENTSK081927RENU MEDICAL OXIMETRY SENSOR, ADULT, PED, INF,NEOK072194RENU REPROCESSED NELLCOR OXIMETRY SENSOR, MODEL D-25, N-25

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Related Devices (Code: JOW)

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.

K261807Sequential Circulator (SC-4004-DL, SC-4008-DL)Bio Compression Systems, Inc.K254217AerloomEvolym, LLCK253555Flexitouch® Plus Advanced Pneumatic Compression SystemTactile MedicalK253386DVT GarmentVistar Medical Supplies Co., Ltd.K250242Compression Therapy Device (LGT-2202DVT)Guangzhou Longest Medical Technology Co., Ltd.K254267NanoPress 760A-BT (760A-BT)Mego Afek , Ltd.

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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