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FDA 510(k)

MODIFIED MODEL 5320 T.E.D. COMPRESSION LIMB

K-Number: K863581 · 1986-10-31

ApplicantThe Kendal Co.
Decision Date1986-10-31
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODIFIED MODEL 5320 T.E.D. COMPRESSION LIMB is the device name listed in this FDA 510(k) record. The listed applicant is The Kendal Co.. It received FDA 510(k) clearance on 1986-10-31 under 510(k) number K863581. 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 MODIFIED MODEL 5320 T.E.D. COMPRESSION LIMB?

MODIFIED MODEL 5320 T.E.D. COMPRESSION LIMB is a medical device that received FDA 510(k) clearance on 1986-10-31. The listed applicant is The Kendal Co.. The 510(k) number is K863581.

When did MODIFIED MODEL 5320 T.E.D. COMPRESSION LIMB receive FDA 510(k) clearance?

MODIFIED MODEL 5320 T.E.D. COMPRESSION LIMB received FDA 510(k) clearance on 1986-10-31, under 510(k) number K863581.

Who is the listed applicant for MODIFIED MODEL 5320 T.E.D. COMPRESSION LIMB?

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

What is the FDA product code for MODIFIED MODEL 5320 T.E.D. COMPRESSION LIMB?

The FDA product code for MODIFIED MODEL 5320 T.E.D. COMPRESSION LIMB is JOW.

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Other records listing The Kendal Co. as applicant

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K000087MARHUKAR TRIPLE LUMEN CATHETER, MODEL 12 FRK990500KENDALL ULTRAMER COUDE FOLEY CATHETER, MODEL 1416C, KENDALL CURITY COUDE FOLEY CATHETER TRAY, MODEL 6946CK991758MONOJECT INSULIN SYRINGEK970969KENDALL CURITY SUPRAPUBIC CATHETER TRAY, KIT, & REPLACEMENT SETK951488KENDALL CURITY CATHETER PLUG WITH PROTECTIVE CAPK942664KENDALL MODEL 6325 SCD SEQUEL COMPRESSION SYSTEM

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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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