← Product Code [IXR](/submissions/RA/subpart-b%E2%80%94diagnostic-devices/IXR) · K965096

# FLUOROVIEW SERIES FLUOROSCOPIC TABLES (K965096)

_U.S. Imaging Tables, Inc. · IXR · Jan 27, 1997 · Radiology · SESE_

**Canonical URL:** https://fda.innolitics.com/submissions/RA/subpart-b%E2%80%94diagnostic-devices/IXR/K965096

## Device Facts

- **Applicant:** U.S. Imaging Tables, Inc.
- **Product Code:** [IXR](/submissions/RA/subpart-b%E2%80%94diagnostic-devices/IXR.md)
- **Decision Date:** Jan 27, 1997
- **Decision:** SESE
- **Submission Type:** Traditional
- **Regulation:** 21 CFR 892.1980
- **Device Class:** Class 2
- **Review Panel:** Radiology

## Intended Use

The Fluoroview™ Series Fluoroscopic Tables (Model 9680) and the Time Table C-Arm Stretcher, Model 9670 is designed for clinical applications such as: to support a patient and facilitate a diagnostic procedure employing some imaging technique or to position a patient for various treatments in clinics or hospitals. This device is used by a physician or a health care professional; this device is not operated by a patient.

## Device Story

Fluoroview™ Series Fluoroscopic Tables (Model 9680) and Time Table C-Arm Stretcher (Model 9670); mechanical patient support systems. Function: position patients to facilitate access for imaging systems or clinical treatments. Operation: manual adjustment by physicians or healthcare professionals in clinical/hospital settings. Benefit: enables patient stabilization and optimal positioning for diagnostic procedures. Device utilizes conventional design and materials consistent with existing fluoroscopic tables.

## Clinical Evidence

Bench testing only; no clinical data provided.

## Technological Characteristics

Mobile fluoroscopic tilting table (21 CFR 892.11980). Mechanical support and adjustment system. Materials and construction are conventional, consistent with industry standards for similar imaging tables.

## Regulatory Identification

A radiologic table is a device intended for medical purposes to support a patient during radiologic procedures. The table may be fixed or tilting and may be electrically powered.

## Special Controls

*Classification.* Class II (special controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to § 892.9.

## Predicate Devices

- Deluxe “C” Arm Stretcher, Model 056-004 (Biodex Medical Systems, Inc.)

## Submission Summary (Full Text)

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JAN 27 1997
K 965096

# EXHIBIT 15

## Summary of Safety & Effectiveness

This device, the *Fluoroview™ Series Fluoroscopic Tables* (Model 9680) and the *Time Table C-Arm Stretcher*, Model 9670 is designed for clinical applications such as: to support a patient and facilitate a diagnostic procedure employing some imaging technique or to position a patient for various treatments in clinics or hospitals. This device is used by a physician or a health care professional; this device is not operated by a patient. This is a Class II device. As such this device has a Classification name as: Mobile Fluoroscopic Tilting Table, as described in 21 CFR Part 892.11980. *U.S. Imaging Tables, Incorporated* has determined this device is substantially equivalent to a predicate medical device which is currently in commerce and is identified as: Deluxe “C” Arm Stretcher, Model 056-004, and is manufactured by Biodex Medical Systems, Inc. of Shirley New York.

A determination of substantial equivalence is based upon the following:

1. This device offers mechanical support and adjustment to suspend and position a patient into various arrangements where various parts of the patient would be accessible to an imaging system.
2. This device uses conventional design, construction and those materials commonly found in most similar Tables. This device uses conventional design, construction and those materials similar to the predicate, substantially equivalent device {except where this device is suited to a more general purpose design}.
3. This device has benefited from design, development, testing and production procedures that conform to Good Manufacturing Procedures.
4. This device has performance characteristics substantially equivalent to its predicate device {which includes differences to facilitate the various clinical applications for which it is intended}.
5. This device is safe and effective for the application for which it is intended and has been tested to confirm its safety and effectiveness.

U.S. Imaging Tables, Incorporated continues to search all appropriate sources for information relating to safety and effectiveness and maintains an in-house reporting system to identify adverse safety and effectiveness information and as such, applicable data is recorded for this device.

## CERTIFICATION:

I hereby certify that this Summary of Safety and Effectiveness applies for the above indicated device.

Date: 11/14/96
Signed by:
Mr. Ronald Denezzo
Acting Operations Manager
U.S. Imaging Tables, Incorporated
28 Central Avenue
Happauge, NY 11788
V-516 231 7300
F-516 231 7542

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**Source:** [https://fda.innolitics.com/submissions/RA/subpart-b%E2%80%94diagnostic-devices/IXR/K965096](https://fda.innolitics.com/submissions/RA/subpart-b%E2%80%94diagnostic-devices/IXR/K965096)

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