Flotation Unit, Chair

FDA 510(k) K760613 · Medpro, Inc.

Substantially Equivalent

510(k) numberK760613

Submission

Device name
Flotation Unit, Chair
Applicant
Medpro, Inc.
Mchenry, IL, US
Received
September 10, 1976
Decision date
October 14, 1976
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
KIC – Cushion, Flotation
Device class
Class I (low risk)
Regulation
21 CFR 890.3175
Specialty
Physical Medicine

Other 510(k)s with product code KIC

510(k)DeviceApplicantDecision
K960189Gel-T CushionKIC · Traditional Span-America Medical Systems, Inc.02/07/1996SE
K953352Proteam CushionKIC · Traditional Iskra.Med11/29/1995SE
K954117Customcare Seating SystemKIC · Traditional Span-America Medical Systems, Inc.10/13/1995SE
K950085Multicure(R) S Gel PadKIC · Traditional Multigestion (Deutschland) GmbH07/13/1995SE
K945667Micos Micropulse(Tm) Alternating Pressure Wheelchair CushionKIC · Traditional Micos Medical Systems02/21/1995SE
K941858Gel CushionKIC · Traditional Hollister, Inc.05/05/1994SE
K911843Zero-G(Tm) Gel/Foam Mattress TopperKIC · Traditional Steridyne Corp.05/30/1991SE
K872739Safe-Seat, Low-Profile Wheelchair CushionKIC · Traditional D.A. Schulman, Inc.07/30/1987SE
K864109C' Airecush Seat CushionKIC · Traditional Medical Industries America, Inc.11/14/1986SE
K864108Push CushKIC · Traditional Medical Industries America, Inc.11/14/1986SE

More from Medical Industries America, Inc.

510(k)DeviceDecision
K772062Neonatal Flotation SystemIKY · Traditional 11/15/1977SE
K771824Medpro Flotation SystemIKY · Traditional 10/19/1977SE
K760870Heel/Elbow Flotation CushionFMP · Traditional 11/01/1976SE

Questions and answers

When was Flotation Unit, Chair cleared by the FDA?

Flotation Unit, Chair (K760613) received a 510(k) decision of Substantially Equivalent on October 14, 1976, 34 days after the submission was received.

What is the product code of K760613?

The FDA product code is KIC – Cushion, Flotation, a Class I (low risk) device regulated under 21 CFR 890.3175.