Vanna Bathing System

FDA 510(k) K993872 · Vancare, Inc.

Substantially Equivalent

510(k) numberK993872

Submission

Device name
Vanna Bathing System
Applicant
Vancare, Inc.
Aurora, NE, US
Received
November 15, 1999
Decision date
February 16, 2000
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
ILJ – Bath, Hydro-Massage
Device class
Class II (moderate risk)
Regulation
21 CFR 890.5100
Specialty
Physical Medicine

Other 510(k)s with product code ILJ

510(k)DeviceApplicantDecision
K110994Parker 500ILJ · Abbreviated Arjohuntleigh, Inc.07/06/2011SE
K082951Immersion HydrobathILJ · Traditional Arjo Hospital Equipment AB04/08/2009SE
K052479Mbath 1000 (60)ILJ · Traditional Enneking Medical, Inc.01/26/2006SE
K040772Pacific Recumbent Height-Adjustable Bath SystemILJ · Traditional Penner Manufacturing, Inc.04/05/2004SE
K012061Superior Bath, Model 6300ILJ · Traditional Penner Manufacturing, Inc.07/19/2001SE
K012057Cascade Bath, Model 6900ILJ · Traditional Penner Manufacturing, Inc.07/19/2001SE
K001079Recumbent Bathing Systems, Rhapsody and PrimoILJ · Traditional Arjo, Inc.05/01/2000SE
K992779A-2000 Bathing Systems; Hydrosonic Bathin SystemILJ · Traditional Medi-Man Rehabilitation Products, Inc.01/13/2000SE
K991184Hydrotone-Thermal Capsule SystemILJ · Abbreviated Nats Corp.06/23/1999SE
K980909Vichy ShowerILJ · Traditional Bouvier Hydro, Inc.08/11/1998SE

Questions and answers

When was Vanna Bathing System cleared by the FDA?

Vanna Bathing System (K993872) received a 510(k) decision of Substantially Equivalent on February 16, 2000, 93 days after the submission was received.

What is the product code of K993872?

The FDA product code is ILJ – Bath, Hydro-Massage, a Class II (moderate risk) device regulated under 21 CFR 890.5100.