VASO PRESS SYSTEM— 510(k) K974393

Substantially Equivalent

Britt Corp., Inc.

FDA 510(k) clearance K974393 for VASO PRESS SYSTEM, Substantially Equivalent on 1999-03-19. Applicant: Britt Corp., Inc.. Device class: 2.

Clearance details

Applicant: Britt Corp., Inc.
Product code: Code JOW
Device class: Class 2
Regulation: 21 CFR 870.5800
Advisory panel: Cardiovascular
Date received: 1997-11-21
Decision date: 1999-03-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Freehold, NJ, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code JOW

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K253555 — Flexitouch® Plus Advanced Pneumatic Compression System2026-07-31
K253386 — DVT Garment2026-06-25
K250242 — Compression Therapy Device (LGT-2202DVT)2026-04-24

More clearances from Britt Corp., Inc.

K003828 — VASO PRESS DVT FOOT GARMENT #VP 5202001-05-18
K991038 — VASO PRESS DVT SYSTEM, MODELS VP500, VP5012000-06-22
K860977 — MODEL 545-45 FOR NEUROLOGICAL SURGICAL APPLICATION1986-10-16
K860975 — MODEL 545-45 LASER FOR EAR, NOSE & THROAT1986-07-18
K860974 — MODEL 545-45 LASER FOR DERMA., POD., SURGICAL1986-07-07

Recalls naming K974393

K-number listed on FDA's recall record

Z-1343-2019 — MediPress pneumatic compression system, Half Leg-Segmental Gradient, Model #6102-SClass II·Terminated·Compass Health Brands (Corporate Office)·20190408
Z-1344-2019 — MediPress pneumatic compression system Full Leg (Medium)-Segmental Gradient, Model #6103M-SClass II·Terminated·Compass Health Brands (Corporate Office)·20190408
Z-1345-2019 — MediPress pneumatic compression system Full Arm (Medium)-Segmental Gradient, Model #6104M-SClass II·Terminated·Compass Health Brands (Corporate Office)·20190408
Z-1346-2019 — MediPress pneumatic compression system Full Leg (Long)-Segmental Gradient, Model #6103L-SClass II·Terminated·Compass Health Brands (Corporate Office)·20190408
Z-1347-2019 — MediPress pneumatic compression system Full Leg (Short)-Segmental Gradient, Model #6103S-SClass II·Terminated·Compass Health Brands (Corporate Office)·20190408
Z-1348-2019 — MediPress pneumatic compression system Full Arm (Short)-Segmental Gradient, Model #6104S-SClass II·Terminated·Compass Health Brands (Corporate Office)·20190408

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K974393.

Data sourced from openFDA. This site is unofficial and independent of the FDA.