Ferno Ille Hi-Lo Jr. Mobile Whirlpool, Model 403

FDA 510(k) K914125 · Ferno

Substantially Equivalent

510(k) numberK914125

Submission

Device name
Ferno Ille Hi-Lo Jr. Mobile Whirlpool, Model 403
Applicant
Ferno
Wilmington, OH, US
Received
September 13, 1991
Decision date
October 25, 1991
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement 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

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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
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K993872Vanna Bathing SystemILJ · Traditional Vancare, Inc.02/16/2000SE
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

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Questions and answers

When was Ferno Ille Hi-Lo Jr. Mobile Whirlpool, Model 403 cleared by the FDA?

Ferno Ille Hi-Lo Jr. Mobile Whirlpool, Model 403 (K914125) received a 510(k) decision of Substantially Equivalent on October 25, 1991, 42 days after the submission was received.

What is the product code of K914125?

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