Kinetic Auto Technic K.A.T. Table
by Buckman Co., Inc. 510(k)
Active
510(k) K851328
Overview
This device is a Table, Physical Therapy, Multi Function as defined in the nomenclature authority. It is identified as the Kinetic Auto Technic K.A.T. Table.
It received FDA 510(k) clearance (K851328) on July 17, 1985, and is classified as a Class II device under regulation number 890.5880. The device is manufactured by Buckman Co., Inc. in Martinez, CA, and is supplied non-sterile for reuse in physical medicine settings.
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK851328 | Date17 Jul 1985 | StatusActive |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not known
- Not covered
United States — FDA 510(k) Active
Recalls
No FDA recalls on record, checked 6 Oct 2026.
Specification
- 510(k) Number
- FDA Product Code
- JFB
- Device Class
- Class II
- Regulation
- 21 CFR Part 890.5880
- Advisory Committee
- Physical Medicine
- FDA Decision
- SESE Substantially Equivalent
Other devices from Buckman Co., Inc.
Questions
What is the Kinetic Auto Technic K.A.T. Table used for?
It is a multi-function table designed for physical therapy applications, providing adjustable positioning and support for patients during therapeutic exercises and treatments in physical medicine settings.
Is the Kinetic Auto Technic K.A.T. Table sterile or non-sterile, and is it intended for single use or reuse?
The device is supplied non-sterile and is designed for reuse after appropriate cleaning and disinfection between patients, as indicated in its labeling and intended use in clinical environments.
What regulatory pathway was used for the Kinetic Auto Technic K.A.T. Table, and what is its classification?
It received FDA 510(k) clearance under submission K851328 on July 17, 1985, and is classified as a Class II medical device under regulation 890.5880 for physical medicine tables.