← Product Code [IYO](/submissions/RA/subpart-b%E2%80%94diagnostic-devices/IYO) · K950943

# ULTRA EASE (K950943)

_Lectec Corp. · IYO · Mar 7, 1996 · Radiology · SESE_

**Canonical URL:** https://fda.innolitics.com/submissions/RA/subpart-b%E2%80%94diagnostic-devices/IYO/K950943

## Device Facts

- **Applicant:** Lectec Corp.
- **Product Code:** [IYO](/submissions/RA/subpart-b%E2%80%94diagnostic-devices/IYO.md)
- **Decision Date:** Mar 7, 1996
- **Decision:** SESE
- **Submission Type:** Traditional
- **Regulation:** 21 CFR 892.1560
- **Device Class:** Class 2
- **Review Panel:** Radiology

## Indications for Use

Ultra Ease Ultrasound Gel Pad is indicated for use as an ultrasound transmission gel to be used in conjunction with an Ultrasonic Blood Flow Detector to auscultate peripheral vascular perfusion.

## Device Story

Ultra Ease Ultrasound Gel Pad; rectangular pad consisting of medical grade foam tape ring, solid hydrogel transmission layer, and polyester film cover. Used as acoustic coupling medium for Ultrasonic Blood Flow Detectors; facilitates ultrasound transmission during auscultation of peripheral vascular perfusion. Applied by clinician to patient skin; replaces traditional liquid gels. Benefits include ease of use, reduced mess, and consistent coupling. Packaged in heat-sealed pouches.

## Clinical Evidence

Bench testing: Primary Skin Irritation Test, Repeated Insult Patch Test (n=50), and Agarose Overlay Cytotoxicity Test. Clinical evaluation confirms effectiveness for intended use as ultrasound transmission medium.

## Technological Characteristics

Rectangular pad; medical grade foam tape ring; solid hydrogel transmission layer; polyester film cover. Non-irritating. Individually packaged in heat-sealed paper/poly/foil/poly pouches.

## Regulatory Identification

An ultrasonic pulsed echo imaging system is a device intended to project a pulsed sound beam into body tissue to determine the depth or location of the tissue interfaces and to measure the duration of an acoustic pulse from the transmitter to the tissue interface and back to the receiver. This generic type of device may include signal analysis and display equipment, patient and equipment supports, component parts, and accessories.

## Special Controls

*Classification.* Class II (special controls). A biopsy needle guide kit intended for use with an ultrasonic pulsed echo imaging system only is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 892.9.

## Predicate Devices

- Aquasonic Ultrasonic Transmission Gel
- Aquaflex Ultrasound Gel Pad

## Submission Summary (Full Text)

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K950943

# Summary of Safety and Effectiveness for Ultra Ease Ultrasound Gel Pad

## I. General Information

Device Generic Name: Ultrasound Gel Pad

Device Trade Name: Ultra Ease Ultrasound Gel Pad

Applicant's Name and Address: LecTec Corporation
10701 Red Circle Drive
Minnetonka, MN 55343

510(k) Number: Unknown

Aquasonic Ultrasonic Transmission Gel and Aquaflex Ultrasound Gel Pad

Parker Laboratories
Orange, New Jersey 07050

Date of Judgement of Substantial Equivalence: Unknown

## II. Description of Conditions for Which the Device is Indicated

Ultra Ease Ultrasound Gel Pad is indicated for use as an ultrasound transmission gel to be used in conjunction with an Ultrasonic Blood Flow Detector to auscultate peripheral vascular perfusion.

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## III. Device Description

Ultra Ease Ultrasound Gel Pad is a non-irritating, rectangular shaped pad, that consists of a medical grade foam tape ring, a solid hydrogel transmission layer, and a polyester film cover. The pads are individually packaged in heat sealed paper/poly/foil/poly pouches.

## IV. Alternatives

Other ultrasound transmission gels are alternatives for the Ultra Ease Ultrasound Gel Pad.

## V. Potential Adverse Effects

Potential adverse effects associated with Ultra Ease Ultrasound Gel Pad are the same as those associated with other ultrasound transmission gels.

## VI. Summary of Studies

Skin contact materials have passed a Primary Skin Irritation Test, a Repeated Insult Patch Tests (on 50 human subjects) and an Agarose Overlay Cytotoxicity Test to demonstrate pad safety. Clinical evaluation shows the pads are effective for the intended use.

## VII. Conclusion

The information presented for the Ultra Ease Ultrasound Gel Pad demonstrates that it will perform in a safe and effective manner, as intended.

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**Source:** [https://fda.innolitics.com/submissions/RA/subpart-b%E2%80%94diagnostic-devices/IYO/K950943](https://fda.innolitics.com/submissions/RA/subpart-b%E2%80%94diagnostic-devices/IYO/K950943)

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