← Product Code [KKO](/submissions/DE/subpart-f%E2%80%94therapeutic-devices/KKO) · K981202 # WATER FILLED GUM SOOTHER (K981202) _Corium Corp. · KKO · Jun 16, 1998 · Dental · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/DE/subpart-f%E2%80%94therapeutic-devices/KKO/K981202 ## Device Facts - **Applicant:** Corium Corp. - **Product Code:** [KKO](/submissions/DE/subpart-f%E2%80%94therapeutic-devices/KKO.md) - **Decision Date:** Jun 16, 1998 - **Decision:** SESE - **Submission Type:** Traditional - **Regulation:** 21 CFR 872.5550 - **Device Class:** Class 2 - **Review Panel:** Dental - **Attributes:** Therapeutic, Pediatric ## Indications for Use The intended use or purpose of the Device is to provide a teething child with a cool soothing effect on the gums when the Device is chewed upon. ## Device Story Water-filled teething ring designed for infants/children experiencing teething discomfort. Device is chilled prior to use; provides cooling sensation to gums when chewed. Used in home environment by child under caregiver supervision. Simple mechanical device; no electronic components or software. ## Clinical Evidence No clinical data; bench testing only. ## Technological Characteristics Water-filled plastic ring; cooling medium is water; intended for oral use; non-sterile; no electronic or software components. ## Regulatory Identification A teething ring is a divice intended for use by infants for medical purposes to soothe gums during the teething process. ## Special Controls *Classification.* Class I if the teething ring does not contain a fluid, such as water. The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter.(2) Class II (special controls) if the teething ring contains a fluid, such as water. The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 872.9. ## 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}------------------------------------------------ Image /page/0/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo features a stylized caduceus symbol, which is a staff with two snakes coiled around it. The words "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" are arranged in a circular pattern around the caduceus symbol. القرب القرب القرب القرب القرب القريب القريب القريب القرن القرن القرن القرن القرن القرن القرن القرن القرن القرن القريب القريب القريب القرن القرن القرن القريب القريب القرن ال Public Health Service Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850 TUN 1 6 1998 Mr. Joseph Hakim ·Contract Manufacturing, Incorporated P.O. Box 4084 Monroe, Louisiana 71211 Re : K981202 Trade Name: Water Filled Gum Soother Requlatory Class: II Product Code: KKO Dated: March 23, 1998 Received: April 2, 1998 ## Dear Mr. Hakim: We have reviewed your Section 510(k) notification of intent to market the device referenced above and we 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). 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 (Premarket Approval), it may be subject to such additional controls. Existing major regulations affecting your device can be found in the Code of Federal Requlations, Title 21, Parts 800 to 895. A substantially equivalent-determination assumes compliance with the Current Good Manufacturing Practice requirements, as set forth in the Quality System Regulation (QS) for Medical Devices: General regulation (21 CFR Part 820) and that, through periodic QS inspections, the Food and Drug Administration (FDA) will verify such assumptions. Failure to comply with the GM regulation may result in regulatory In addition, FDA may publish further announcements action. concerning your device in the Federal Reqister. Please note: this response to your premarket notification submission does not affect any obligation you might have under sections 531 {1}------------------------------------------------ Page 2 - Mr. Hakim through 542 of the Act for devices under the Electronic Product Radiation Control provisions, or other Federal laws or requlations. This letter will allow you to begin marketing your device as described in your 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 requlation (21 CFR Part 801 and additionally 809.10 for in vitro diagnostic devices), please contact the Office of Compliance at (301) 594-4692. Additionally, for questions on the promotion and advertising of your device, please contact the Office of Compliance at (301) 594-4639. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR 807.97). Other general information on your responsibilities under the Act may be obtained from the Division of Small Manufacturers 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 yours, Timothy A. Ulatowski Director Division of Dental, Infection Control, and General Hospital Devices Office of Device Evaluation Center for Devices and Radiological Health ------------------------------------------------------------------------------------------------------------------------------------------------------------------------------ Enclosure ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤﺪﺓ ﺍﻟﻤﺘﺤ {2}------------------------------------------------ Image /page/2/Picture/0 description: The image shows the logo for Contract Manufacturing, Inc. The text is in a bold, sans-serif font. The word "Contract" is on the top line, and the word "Manufacturing" is on the second line. The word "Inc." is on the third line, to the right of the word "Manufacturing." ## INDICATIONS FOR USE , 510(k) Number: K981202 _______________________________________________________________________________________________________________________________________________________ Device Name: Teething Ring - Water Filled Indications For Use: : 上一 The intended use or purpose of the Device is to provide a teething child with a cool soothing effect on the gums when the Device is chewed upon. " | 房 (PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of DRRH, Office of Device Evaluation (ODE) ![Signature](signature.png) (Division Sign-Off) Division of Dental, Infection Control, and General Hospital Devices | 510(k) Number | K981202 | |---------------|---------| |---------------|---------| | Prescription Use Checkmark | OR | Over-The-Counter Use ______ | |-------------------------------------------------------------|-----|-----------------------------| | (Per 21 CFR 801.109) | -6- | (Optional Format 1-2-96) | --- **Source:** [https://fda.innolitics.com/submissions/DE/subpart-f%E2%80%94therapeutic-devices/KKO/K981202](https://fda.innolitics.com/submissions/DE/subpart-f%E2%80%94therapeutic-devices/KKO/K981202) **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