Table, Exam & Manupulation

FDA 510(k) K770636 · I E Industries

Substantially Equivalent

510(k) numberK770636

Submission

Device name
Table, Exam & Manupulation
Applicant
I E Industries
Mchenry, IL, US
Received
April 4, 1977
Decision date
April 15, 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
K770609Table, Massage & Treatmhnt, Fixed HeightINT · Traditional Will Ross Co.04/08/1977SE
K770509Table, Massage and TreatmentINT · Traditional Will Ross Co.04/05/1977SE

More from Will Ross Co.

510(k)DeviceDecision
K770438Cart, ProceduresHDD · Traditional 07/01/1977SE
K770437Table, ExaminationKNC · Traditional 03/23/1977SE

Questions and answers

When was Table, Exam & Manupulation cleared by the FDA?

Table, Exam & Manupulation (K770636) received a 510(k) decision of Substantially Equivalent on April 15, 1977, 11 days after the submission was received.

What is the product code of K770636?

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