Reusable Adult Incontinent Diaper
FDA 510(k) K883787 · Intera Corp.
510(k) numberK883787
Submission
- Device name
- Reusable Adult Incontinent Diaper
- Applicant
- Intera Corp.
Chattanooga, TN, US - Received
- September 7, 1988
- Decision date
- November 7, 1988
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- EYQ – Garment, Protective, For Incontinence
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 876.5920
- Specialty
- Gastroenterology, Urology
Other 510(k)s with product code EYQ
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K950784 | Dristar Urinary Incontinence Management SystemEYQ · Traditional | Advanced Bioresearch Assoc. | 05/03/1995SE |
| K932310 | Kit Pak Incontinent Skin Care KitEYQ · Traditional | Kit Pak, Inc. | 06/01/1994SEKD |
| K903342 | Deodorizing and Sound Muffling Anal PadEYQ · Traditional | Biological Resistance, Inc. | 10/23/1990SE |
| K891686 | Lib System, Baby/Adult DiaperEYQ · Traditional | Intera Corp. | 05/31/1989SE |
| K885185 | Intera Shield and Intera UndergarmentEYQ · Traditional | Intera Corp. | 02/08/1989SE |
| K883895 | Dripride Ultra Incontinent PadEYQ · Traditional | Weyerhaeuser Co. | 01/30/1989SE |
| K883894 | Dripride Provide SlimEYQ · Traditional | Weyerhaeuser Co. | 01/30/1989SE |
| K882418 | Dry Comfort UndergarmentEYQ · Traditional | Health Tec, Inc. | 09/29/1988SE |
| K880454 | At Ease Stress PadEYQ · Traditional | Hospital Specialty Co. | 06/16/1988SE |
| K880455 | At Ease Adult DiaperEYQ · Traditional | Hospital Specialty Co. | 04/14/1988SE |
More from Hospital Specialty Co.
| 510(k) | Device | Decision |
|---|---|---|
| K891686 | Lib System, Baby/Adult DiaperEYQ · Traditional | 05/31/1989SE |
| K885185 | Intera Shield and Intera UndergarmentEYQ · Traditional | 02/08/1989SE |
| K883424 | Surgical Gown/Scrub/Laparotomy/Mayo Stand/Back TabKKX · Traditional | 09/06/1988SE |
| K863732 | Surgical Drape & Drape AccessoriesKKX · Traditional | 10/23/1986SE |
| K862380 | Mattress CoverEYQ · Traditional | 07/28/1986SE |
Questions and answers
When was Reusable Adult Incontinent Diaper cleared by the FDA?
Reusable Adult Incontinent Diaper (K883787) received a 510(k) decision of Substantially Equivalent on November 7, 1988, 61 days after the submission was received.
What is the product code of K883787?
The FDA product code is EYQ – Garment, Protective, For Incontinence, a Class I (low risk) device regulated under 21 CFR 876.5920.