← Product Code [GYB](/submissions/NE/subpart-b%E2%80%94neurological-diagnostic-devices/GYB) · K032239 # THERA-CREAM, MODEL TCT004 (K032239) _Prizm Medical, Inc. · GYB · Jul 30, 2004 · Neurology · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/NE/subpart-b%E2%80%94neurological-diagnostic-devices/GYB/K032239 ## Device Facts - **Applicant:** Prizm Medical, Inc. - **Product Code:** [GYB](/submissions/NE/subpart-b%E2%80%94neurological-diagnostic-devices/GYB.md) - **Decision Date:** Jul 30, 2004 - **Decision:** SESE - **Submission Type:** Traditional - **Regulation:** 21 CFR 882.1275 - **Device Class:** Class 2 - **Review Panel:** Neurology - **Attributes:** Therapeutic ## Indications for Use Thera-Cream™ is a conductive cream, which increases skin conductivity for electrotherapy treatment and was developed for use with the Prizm brand electrotherapy units and the Intelligent Textiles® brand of garment electrodes. ## Device Story Thera-Cream™ is a topical electroconductive cream applied to skin prior to placement of garment electrodes. It contains conductive copper salts to reduce skin impedance and increase conductivity for TENS and NMES electrotherapy. The cream base provides a moisturizing effect. It is intended for use by patients or clinicians in conjunction with Prizm brand electrotherapy units and Intelligent Textiles® garment electrodes. By improving electrical contact, the device facilitates effective delivery of therapeutic electrical stimulation. ## Clinical Evidence No clinical data provided; bench testing only. ## Technological Characteristics Electroconductive medium; contains conductive copper salts in a moisturizing cream base. Designed for topical application to skin to interface with garment electrodes. Class II device (21 CFR 882.1275). ## Regulatory Identification Electroconductive media are the conductive creams or gels used with external electrodes to reduce the impedance (resistance to alternating current) of the contact between the electrode surface and the skin. ## Predicate Devices - Conduct-Mist™ ([K024181](/device/K024181.md), [K951727](/device/K951727.md)) - Conductive Aloe Vera Gel ([K925466](/device/K925466.md)) - SignaCreme® ([K782055](/device/K782055.md)) - Ultra/Phonic White (Preamendment) - ReliefBand® Conductivity Gel ([K020180](/device/K020180.md)) ## Submission Summary (Full Text) > This content was OCRed from public FDA records by [Innolitics](https://innolitics.com). If you use, quote, summarize, crawl, or train on this content, cite Innolitics at https://innolitics.com. > > Innolitics is a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices, including [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/). {0}------------------------------------------------ # Prizm Medical, Inc. Thera-Cream™ 510(k) # K032239 # JUL 3 0 2004 ## Attachment 2 ## 510(k) Summary - Revised | Submitted By: | Prizm Medical, Inc.
3400 Corporate Way, Suite I
Duluth, GA 30096 | Phone: (770) 622-0933
Fax: (770) 622-9392 | |----------------------------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|----------------------------------------------| | Contact Person: | Julie Stephens | | | Date Prepared: | 05/18/04 | | | Trade/Proprietary Name: | Thera-Cream™ | | | Common Name: | Electroconductive Cream | | | Classification Name: | Electroconductive Media (21 CFR 882.1275) | | | Product Code: | GYB, Neurology | | | Legally Marketed
Predicate Devices: | Conduct-Mist™ - 510(k) Numbers: K024181 & K951727;
Conductive Aloe Vera Gel - 510(k) Number: K925466;
SignaCreme® - 510(k) Number: K782055; Ultra/Phonic White
- Preamendment; ReliefBand® Conductivity Gel: 510(k)
Number K020180 | | ## Device Description: The Prizm Medical Inc.'s Thera-Cream™ product is used prior to electrode placement to reduce the impedance (resistance to alternating current), which increases the skin conductivity during electrotherapy treatment. Electrotherapy treatment includes the use of TENS (Transcutaneous Electrical Nerve Stimulators) and NMES (Neuromuscular Electrical Stimulators). #### Intended Use: Thera-Cream™ is a conductive cream, which increases skin conductivity for electrotherapy treatment and was developed for use with the Prizm brand electrotherapy units and the Intelligent Textiles® brand of garment electrodes. ## Similarities and Differences of the Thera-Cream™ product to the Predicate Device: #### Similarities The Prizm Medical Inc.'s Thera-Cream™ product has the same intended use as the predicate products. Specifically, both the Conduct-Mist™ product and the Thera-Cream™ product use "conductive copper salts" which "increases the skin conductivity". {1}------------------------------------------------ # Attachment 2 (Continued) # 510(k) Summary - Revised ### Differences The Prizm Medical Inc.'s Thera-Cream™ product utilizes a "moisturizing cream base" combined with the "conductive copper salts" that is rubbed onto the skin surface prior to garment electrode placement. The Conduct-Mist™ product utilizes a liquid/water base combined with the "conductive copper salts" that can be sprayed on the skin surface prior to garment electrode placement. The Prizm Medical Inc.'s Thera-Cream™ product utilizes a "moisturizing cream base" which moisturizes skin. The Conduct-Mist™ product does not contain moisturizing ingredients. {2}------------------------------------------------ Image /page/2/Picture/1 description: The image shows a seal or logo. The logo is circular and contains text around the perimeter. The text reads "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA". In the center of the logo is an abstract symbol that resembles an eagle or bird with three curved lines representing its wings. Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850 JUL 3 0 2004 Prizm Medical, Inc. C/o Ms. Julie Stephens Regulatory Resources Group, Inc. 111 Laurel Ridge Drive Alpharetta, Georgia 30004 Re: K032239 Trade/Device Name: Thera-Cream™ Regulation Number: 21 CFR 882.1275 Regulation Name: Electroconductive media Regulatory Class: II Product Code: GYB Dated: May 18, 2004 Received: May 19, 2004 Dear Ms. Stephens: We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (Act) that do not require approval of a premarket approval application (PMA), You may, therefore, market the device, subject to the general controls provisions of the Act. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration. If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to such additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register. Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050. {3}------------------------------------------------ Page 2 - Ms. Julie Stephens This letter will allow you to begin marketing your device as described in your Section 510(k) premarket notification. The FDA finding of substantial equivalence of your device to a legally marketed predicate device results in a classification for your device and thus, permits your device to proceed to the market. If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please contact the Office of Compliance at (301) 594-4659. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). You may obtain other general information on your responsibilities under the Act from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number (800) 638-2041 or (301) 443-6597 or at its Internet address http://www.fda.gov/cdrh/dsma/dsmamain.html Sincerely vours. Mark A. Milliken Celia M. Witten, Ph.D., M.D. Director Division of General, Restorative and Neurological Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {4}------------------------------------------------ # Indications for Use 510(k) Number (if known): K032239 Device Name: Prizm Medical, Inc. Thera-Cream™ Indications for Use: Thera-Cream™ is a conductive cream, which increases skin conductivity for electrotherapy Thera-Cream - 15 a bonuted for use with the Prizm brand electrotherapy units and the Intelligent Textiles® brand of garment electrodes. Prescription Use _ x (Part 21 CFR 801 Subpart D) AND/OR Over-The-Counter Use (21 CFR 807 Subpart C) (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE OF NEEDED) Concurrence of CDRH, Office of Device Evaluation (ODE) Mark N. Mulhearn (Division Sign-Off) Division of General, Restorative, and Neurological Devices Page 1 of 1 **510(k) Number** K032234 --- **Source:** [https://fda.innolitics.com/submissions/NE/subpart-b%E2%80%94neurological-diagnostic-devices/GYB/K032239](https://fda.innolitics.com/submissions/NE/subpart-b%E2%80%94neurological-diagnostic-devices/GYB/K032239) **Published by [Innolitics](https://innolitics.com)** — a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices. If you're preparing [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/), [get in touch](https://innolitics.com/contact). **Cite:** Innolitics at https://innolitics.com