Stroke Sling

FDA 510(k) K771031 · Stat Medical Corp.

Substantially Equivalent

510(k) numberK771031

Submission

Device name
Stroke Sling
Applicant
Stat Medical Corp.
Mchenry, IL, US
Received
June 9, 1977
Decision date
June 27, 1977
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
ILI – Sling, Arm
Device class
Class I (low risk)
Regulation
21 CFR 890.3640
Specialty
Physical Medicine

Other 510(k)s with product code ILI

510(k)DeviceApplicantDecision
K912661Matrx, Pyramid Triangle BandageILI · Traditional Matrix Medica, Inc.08/21/1991SE
K831549Arm SlingsILI · Traditional Fred Sammons, Inc.06/30/1983SE
K831706Sato Family First Aid KitILI · Traditional Food and Drug Service, Inc.06/24/1983SE
K823810A.C. SplintILI · Traditional Danek Medical, Inc.01/14/1983SE
K823808Various Arm SlingILI · Traditional Danek Medical, Inc.01/14/1983SE
K823664Universal Sling, Sling & SwatheILI · Traditional Warm & Form, Orthopedic Materials12/30/1982SE
K823162Universal Sling, Sling & SwatheILI · Traditional Warm & Form, Orthopedic Materials11/10/1982SE
K820590Orthopedic Soft GoodsILI · Traditional Abco Dealers, Inc.03/26/1982SE
K812480Limb Holder Arm SlingILI · Traditional Maddak, Inc.09/14/1981SE
K812478Maddacomfort SlingILI · Traditional Maddak, Inc.09/14/1981SE

More from Maddak, Inc.

510(k)DeviceDecision
K780171Elbow ProtectorFMP · Traditional 02/06/1978SE
K771030Flexion MittensIOD · Traditional 06/27/1977SE
K770853Sterile CottonFRL · Traditional 05/23/1977SE

Questions and answers

When was Stroke Sling cleared by the FDA?

Stroke Sling (K771031) received a 510(k) decision of Substantially Equivalent on June 27, 1977, 18 days after the submission was received.

What is the product code of K771031?

The FDA product code is ILI – Sling, Arm, a Class I (low risk) device regulated under 21 CFR 890.3640.