Cleared Traditional

K000147 - CTC DVT-1 CALF GARMENT, MODEL DVT-1

K000147 is an FDA 510(k) clearance for CTC DVT-1 CALF GARMENT, manufactured by Compression Therapy Concepts, Inc.. The device is a Class 2 Cardiovascular device with product code JOW cleared through the Traditional 510(k) pathway after a 86-day FDA review.

K000147 · Compression Therapy Concepts, Inc. · Cardiovascular device
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Apr 2000
Decision
86d
Days
Class 2
Risk

K000147 is an FDA 510(k) clearance for the CTC DVT-1 CALF GARMENT, MODEL DVT-1. Classified as Sleeve, Limb, Compressible (product code JOW), Class II - Special Controls.

Submitted by Compression Therapy Concepts, Inc. (South Plainfield, US). The FDA issued a Cleared decision on April 13, 2000 after a review of 86 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.

View all Compression Therapy Concepts, Inc. devices

FDA 510(k) Submission Details - K000147

510(k) Number K000147 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 18, 2000
Decision Date April 13, 2000
Days to Decision 86 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
39d faster than avg
Panel avg: 125d · This submission: 86d
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 140
Devices cleared under the same product code (JOW) and FDA review panel - the closest regulatory comparables to K000147.
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K980600 · Dideco S.P.A. · Aug 1998
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K963067 · Gaymar Industries, Inc. · Jan 1997