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FDA 510(k)

KENDALL MODEL 7325 SCD RESPONSE COMPRESSION SYSTEM, MODEL 7325

K-Number: K992079 · 1999-09-29

ApplicantThe Kendall Company, L.P.
Decision Date1999-09-29
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

KENDALL MODEL 7325 SCD RESPONSE COMPRESSION SYSTEM, MODEL 7325 is the device name listed in this FDA 510(k) record. The listed applicant is The Kendall Company, L.P.. It received FDA 510(k) clearance on 1999-09-29 under 510(k) number K992079. 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 KENDALL MODEL 7325 SCD RESPONSE COMPRESSION SYSTEM, MODEL 7325?

KENDALL MODEL 7325 SCD RESPONSE COMPRESSION SYSTEM, MODEL 7325 is a medical device that received FDA 510(k) clearance on 1999-09-29. The listed applicant is The Kendall Company, L.P.. The 510(k) number is K992079.

When did KENDALL MODEL 7325 SCD RESPONSE COMPRESSION SYSTEM, MODEL 7325 receive FDA 510(k) clearance?

KENDALL MODEL 7325 SCD RESPONSE COMPRESSION SYSTEM, MODEL 7325 received FDA 510(k) clearance on 1999-09-29, under 510(k) number K992079.

Who is the listed applicant for KENDALL MODEL 7325 SCD RESPONSE COMPRESSION SYSTEM, MODEL 7325?

The FDA 510(k) record lists The Kendall Company, L.P. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KENDALL MODEL 7325 SCD RESPONSE COMPRESSION SYSTEM, MODEL 7325?

The FDA product code for KENDALL MODEL 7325 SCD RESPONSE COMPRESSION SYSTEM, MODEL 7325 is JOW.

Related Clinical Trials

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.

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Other records listing The Kendall Company, L.P. 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.

K990530KERLIX MD ANTIMICROBIAL GAUZE DRESSING

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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