Cleared Traditional

K932835 - KENDALL T.E.D./SCD SEQUENTIAL COMPRESSION DEVICE

K932835 is an FDA 510(k) clearance for KENDALL T.E.D./SCD SEQUENTIAL COMPRESSI..., manufactured by Kendall Healthcare Products Co. Div.Of Tyco Health. The device is a Class 2 Cardiovascular device with product code JOW cleared through the Traditional 510(k) pathway after a 57-day FDA review.

K932835 · Kendall Healthcare Products Co. Div.Of Tyco Health · Cardiovascular device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Aug 1993
Decision
57d
Days
Class 2
Risk

K932835 is an FDA 510(k) clearance for the KENDALL T.E.D./SCD SEQUENTIAL COMPRESSION DEVICE. Classified as Sleeve, Limb, Compressible (product code JOW), Class II - Special Controls.

Submitted by Kendall Healthcare Products Co. Div.Of Tyco Health (Mansfield, US). The FDA issued a Cleared decision on August 6, 1993 after a review of 57 days - a notably fast clearance 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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

FDA 510(k) Submission Details - K932835

510(k) Number K932835 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 10, 1993
Decision Date August 06, 1993
Days to Decision 57 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
68d faster than avg
Panel avg: 125d · This submission: 57d
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 336
Devices cleared under the same product code (JOW) and FDA review panel - the closest regulatory comparables to K932835.
INTERMITTENT COMPRESSION SYSTEM MODEL 5000
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K932900 · Aircast, Inc. · Oct 1993
SCD(R) CONTROLLER
K933259 · Kendall Healthcare Products Co. Div.Of Tyco Health · Sep 1993
COWBOY III
K932215 · Kinetic Concepts, Inc. · Jul 1993
PLEXUS PULSER I, PLEXUS PULSER II
K924891 · Dobre, Inc. · Jun 1993
CALF GARMENT DVT10(S) COMPRESSIBLE LIMB SLEEVE
K925717 · Huntleigh Healthcare, Inc. · May 1993