Cleared Traditional

K012614 - KENDALL, SEQUENTIAL COMPRESSION DEVICE

Also marketed or referenced as:
HUNTLEIGH, FLOWTRON VENAFLOW ACUFEX ALPS SHEEPSKIN

K012614 is an FDA 510(k) clearance for KENDALL, manufactured by Medical Instruments Technology, Inc.. The device is a Class 2 Cardiovascular device with product code JOW cleared through the Traditional 510(k) pathway after a 261-day FDA review.

K012614 · Medical Instruments Technology, Inc. · Cardiovascular device
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
May 2002
Decision
261d
Days
Class 2
Risk

K012614 is an FDA 510(k) clearance for the KENDALL, SEQUENTIAL COMPRESSION DEVICE. Classified as Sleeve, Limb, Compressible (product code JOW), Class II - Special Controls.

Submitted by Medical Instruments Technology, Inc. (St. George, US). The FDA issued a Cleared decision on May 1, 2002 after a review of 261 days - an extended review cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.5800 - the FDA cardiovascular device oversight framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Cardiovascular review framework, consistent with the majority of Class II 510(k) submissions.

FDA 510(k) Submission Details - K012614

510(k) Number K012614 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 13, 2001
Decision Date May 01, 2002
Days to Decision 261 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
136d slower than avg
Panel avg: 125d · This submission: 261d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

JOW Device Classification - Class 2, Special Controls

Product Code JOW Sleeve, Limb, Compressible
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.5800
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Cardiovascular devices follow this clearance model.

Regulatory Peers - JOW Sleeve, Limb, Compressible

All 352
Devices cleared under the same product code (JOW) and FDA review panel - the closest regulatory comparables to K012614.
AIRCAST, MODEL #3011
K013297 · Millenium Reprocessing Services, Inc. · Jun 2002
REPROCESSED COMPRESSION LIMB SLEEVES
K012658 · Surgical Instruments Service and Savings, Inc. · May 2002
COMPRESSIBLE LIMB SLEEVE
K012979 · Medical Device Services, Inc. · May 2002
HYGIA HEALTH SERVICES REPROCESSED NUTECH FOOT WRAP
K012650 · Hygia Health Services, Inc. · Apr 2002
HYGIA HEALTH SERVICES REPROCESSED HUNTLEIGH FOOT WRAP MODELS FG 100, FG 200
K012651 · Hygia Health Services, Inc. · Apr 2002
HYGIA HEALTH SERVICES REPROCESSED HUNTLEIGH FLOWTRON DVT SLEEVE MODELS DVT10, DVT 20, DVT 30, DVT 40
K012654 · Hygia Health Services, Inc. · Apr 2002
K012614 · KENDALL, SEQUENTIAL COMPRESSION DEVICE
Download PDF FDA Summary Medical Instruments T…