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FDA 510(k)

RECOVERY+ MODEL PS 511, DVTHERAPY MODEL PS 511A

K-Number: K111748 · 2011-11-23

ApplicantJoy Long
Decision Date2011-11-23
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

RECOVERY+ MODEL PS 511, DVTHERAPY MODEL PS 511A is the device name listed in this FDA 510(k) record. The listed applicant is Joy Long. It received FDA 510(k) clearance on 2011-11-23 under 510(k) number K111748. 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 RECOVERY+ MODEL PS 511, DVTHERAPY MODEL PS 511A?

RECOVERY+ MODEL PS 511, DVTHERAPY MODEL PS 511A is a medical device that received FDA 510(k) clearance on 2011-11-23. The listed applicant is Joy Long. The 510(k) number is K111748.

When did RECOVERY+ MODEL PS 511, DVTHERAPY MODEL PS 511A receive FDA 510(k) clearance?

RECOVERY+ MODEL PS 511, DVTHERAPY MODEL PS 511A received FDA 510(k) clearance on 2011-11-23, under 510(k) number K111748.

Who is the listed applicant for RECOVERY+ MODEL PS 511, DVTHERAPY MODEL PS 511A?

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

What is the FDA product code for RECOVERY+ MODEL PS 511, DVTHERAPY MODEL PS 511A?

The FDA product code for RECOVERY+ MODEL PS 511, DVTHERAPY MODEL PS 511A is JOW.

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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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