Allevyn Dressing Claims Change
FDA 510(k) K904412 · Smith & Nephew United, Inc.
510(k) numberK904412
Submission
- Device name
- Allevyn Dressing Claims Change
- Applicant
- Smith & Nephew United, Inc.
Largo, FL, US - Received
- September 26, 1990
- Decision date
- October 23, 1990
- Decision
- Substantially Equivalent for Some Indications (SN)
- Type
- Traditional 510(k)
Device classification
- Product code
- KOZ – Beads, Hydrophilic, For Wound Exudate Absorption
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 878.4018
- Specialty
- General, Plastic Surgery
Other 510(k)s with product code KOZ
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K905206 | Incare Pinsite DressingKOZ · Traditional | Hollister, Inc. | 04/12/1991SE |
| K905688 | Cutinova HydroKOZ · Traditional | Beiersdorf, Inc. | 04/01/1991SE |
| K905069 | Iodosorb GelKOZ · Traditional | Perstorp AB C/O Robert Joel Slomoff | 01/31/1991SE |
| K904604 | Redi-Release Absorbent DressingKOZ · Traditional | Fountain Pharmaceuticals, Inc. | 01/07/1991SE |
| K903645 | Dermasorb Wound Contact Layer DressingKOZ · Traditional | Convatec, A Division of E.R. Squibb & Sons | 11/21/1990SE |
| K896828 | Bioclusive(R) Absorbent DressingKOZ · Traditional | Johnson & Johnson International | 11/21/1990SE |
| K901876 | Intrasite Cavity Wound Dressing (Label Revision)KOZ · Traditional | Smith & Nephew United, Inc. | 06/28/1990SN |
| K896176 | Exusorb(Tm) Dry/Wet DressingKOZ · Traditional | Controlled Therapeutics Corp. | 11/24/1989SE |
| K895354 | Intrasite Cavity Wound DressingKOZ · Traditional | Smith & Nephew United, Inc. | 11/07/1989SN |
| K874552 | Envisan PadKOZ · Traditional | Marion Laboratories, Inc. | 01/22/1988SN |
More from Marion Laboratories, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K963096 | Allevyn Hydro Poly Dressing ND All Trac DressingKMF · Traditional | 10/25/1996SE |
| K961775 | Profore Four-Layer Bandage System KitEFQ · Traditional | 07/16/1996SE |
| K945330 | Allevyn AdhesiveKMF · Traditional | 02/09/1995SN |
| K943619 | Cavi-Care Conforming Foam DressingKMF · Traditional | 08/19/1994SN |
| K942748 | IntrasiteNAE · Traditional | 06/29/1994SN |
| K935705 | Allevyn Island Wound DressingNAE · Traditional | 02/15/1994SE |
| K935803 | Cica-Care Silicone Gel SheetMDA · Traditional | 02/03/1994SE |
| K932263 | Solosite Dermal Wound GelMGQ · Traditional | 10/01/1993SE |
| K926508 | Intrasite GelNAE · Traditional | 07/13/1993SE |
| K922897 | StrappalKGX · Traditional | 09/15/1992SE |
Questions and answers
When was Allevyn Dressing Claims Change cleared by the FDA?
Allevyn Dressing Claims Change (K904412) received a 510(k) decision of Substantially Equivalent for Some Indications on October 23, 1990, 27 days after the submission was received.
What is the product code of K904412?
The FDA product code is KOZ – Beads, Hydrophilic, For Wound Exudate Absorption, a Class I (low risk) device regulated under 21 CFR 878.4018.