Multi-Flex Table Model 103
by Slenderizers Equipment Mfg., Inc.
510(k) K870712
Active
Valid until
No expiry
FDA recalls
None foundDocuments
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK870712 | Date9 Jun 1987 | StatusActive |
Recalls
No FDA recalls found in the data synced 5 Oct 2026.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
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
Overview
AI-generated summary, 1 Oct 2026
The Multi-Flex Table Model 103 is a multi-function table designed for physical therapy applications, classified under the FDA product code JFB. It is intended for use in physical medicine settings, providing adjustable positioning and support for therapeutic interventions. This device falls under the broader category of tables used in rehabilitation and physical therapy environments, offering flexibility in patient positioning and treatment configurations.
The Multi-Flex Table Model 103 is supplied as a reusable medical device and is regulated under the FDA’s 510(k) clearance process, with a clearance number K870712. It is intended for use in clinical settings where adjustable patient positioning is required, such as physical therapy clinics or rehabilitation centers. The device adheres to regulatory standards outlined in 21 CFR 890.5880 and is classified as a Class II medical device. No specific sterility or MRI safety information is provided in the available data.
Other devices from Slenderizers Equipment Mfg., Inc.
Questions
AI-generated answers, 1 Oct 2026
What is the Multi-Flex Table Model 103 used for?
The Multi-Flex Table Model 103 is a multi-function table specifically designed for physical therapy applications. It provides adjustable positioning and support to facilitate therapeutic interventions in clinical settings like physical medicine clinics or rehabilitation centers. Its flexibility in patient positioning helps clinicians tailor treatments to individual patient needs.
Is the Multi-Flex Table Model 103 reusable or single-use?
The Multi-Flex Table Model 103 is supplied as a reusable medical device. Unlike single-use items, this table is intended for repeated use in clinical environments, provided it is properly cleaned and maintained between patients to ensure hygiene and functionality.
What regulatory approval does the Multi-Flex Table Model 103 have?
The Multi-Flex Table Model 103 has received FDA 510(k) clearance under the clearance number K870712. This classification indicates that the device has been determined to be substantially equivalent to a legally marketed device and adheres to regulatory standards outlined in 21 CFR 890.5880. It is classified as a Class II medical device.
What are the key specifications or features of the Multi-Flex Table Model 103?
The Multi-Flex Table Model 103 is categorized under FDA product code JFB and is intended for use in physical medicine settings. While specific technical details like dimensions or weight are not provided in the available data, its primary feature is adjustable positioning for therapeutic use. The device is regulated under the Physical Medicine advisory committee and is designed to support a variety of rehabilitation treatments.
How should the Multi-Flex Table Model 103 be stored?
While the provided data does not specify storage instructions, reusable medical devices like the Multi-Flex Table Model 103 should generally be stored in a clean, dry environment to prevent damage or contamination. It should be kept in a location that protects it from physical stress, extreme temperatures, and direct sunlight. Proper storage ensures the device remains functional and ready for use when needed.