Table, Massage and Treatment

FDA 510(k) K770509 · Will Ross Co.

Substantially Equivalent

510(k) numberK770509

Submission

Device name
Table, Massage and Treatment
Applicant
Will Ross Co.
Mchenry, IL, US
Received
March 17, 1977
Decision date
April 5, 1977
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
INT – Plinth
Device class
Class I (low risk)
Regulation
21 CFR 890.3520
Specialty
Physical Medicine

Other 510(k)s with product code INT

510(k)DeviceApplicantDecision
K770723Table, Treatment, Therapy, PhysicalINT · Traditional Chattanooga Pharmacal Co.07/11/1977SE
K770636Table, Exam & ManupulationINT · Traditional I E Industries04/15/1977SE
K770609Table, Massage & Treatmhnt, Fixed HeightINT · Traditional Will Ross Co.04/08/1977SE

More from Will Ross Co.

510(k)DeviceDecision
K780850Searle Neonatal Oxygen ProbeCCE · Traditional 08/23/1978SE
K771561Dover Urine MeterEXR · Traditional 09/07/1977SE
K771132Kenwood Biological Steoiliz. IndicatorFRC · Traditional 07/14/1977SE
K770612Splint, BohlerIQI · Traditional 04/08/1977SE
K770611Parallel BarsIOE · Traditional 04/08/1977SE
K770610Table, Treatment & Traction, Hi-LoITH · Traditional 04/08/1977SE
K770609Table, Massage & Treatmhnt, Fixed HeightINT · Traditional 04/08/1977SE
K770608Walking AidITJ · Traditional 04/08/1977SE
K770607Traction HarnessILZ · Traditional 04/08/1977SE
K770399Valve for Closed Sys. Urinary DrainageKNX · Traditional 03/09/1977SE

Questions and answers

When was Table, Massage and Treatment cleared by the FDA?

Table, Massage and Treatment (K770509) received a 510(k) decision of Substantially Equivalent on April 5, 1977, 19 days after the submission was received.

What is the product code of K770509?

The FDA product code is INT – Plinth, a Class I (low risk) device regulated under 21 CFR 890.3520.