Burn Dressing
FDA 510(k) K923846 · Medical Action Industries, Inc.
510(k) numberK923846
Submission
- Device name
- Burn Dressing
- Applicant
- Medical Action Industries, Inc.
Farmingdale, NY, US - Received
- July 31, 1992
- Decision date
- September 11, 1992
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
Device classification
- Product code
- NAB – Gauze / Sponge,Nonresorbable For External Use
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 878.4014
- Specialty
- General, Plastic Surgery
Other 510(k)s with product code NAB
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K946015 | Ivalon External SpongeNAB · Traditional | Ivalon | 02/27/1995SE |
| K940755 | Isolyer (4X4, 8PLY)NAB · Traditional | Isolyer Co. | 05/02/1994SE |
| K931610 | Omnisorb II, Nonwoven Sponge, Sterile and NonNAB · Traditional | Omni Mfg., Inc. | 06/24/1993SE |
| K925590 | Multi-Trauma DressingNAB · Traditional | Gam Industries, Inc. | 04/08/1993SE |
| K926072 | K-Band and K-CrepeNAB · Traditional | Parema , Ltd. | 03/19/1993SE |
| K915591 | Sterile Gauze PadsNAB · Traditional | Eagle Medical, Inc. | 01/27/1993SE |
| K924650 | Gauze SpongesNAB · Traditional | Dav-Mar Medical Products, Inc. | 01/11/1993SE |
| K923602 | Absorbent Pad -- ModificationNAB · Traditional | Winfield Laboratories, Inc. | 12/07/1992SE |
| K923115 | ClinisorbNAB · Traditional | Hermitage Hospital Products, Inc. | 11/23/1992SE |
| K923378 | Usp Type Vii Gauze SpongesNAB · Traditional | E.W.A., Ltd. | 10/06/1992SE |
More from E.W.A., Ltd.
| 510(k) | Device | Decision |
|---|---|---|
| K042526 | Drape, Surgical, X-Ray Element, Models Non Sterile 6120-00, Sterile 704-B, Non Sterile…KKX · Traditional | 04/25/2005SE |
| K042527 | Spatula, Cervical, Cytological, Model 22-9107HHT · Traditional | 11/08/2004SE |
| K022948 | Vaginal Speculum, Model 5555S, 5555M, or 5555LHIB · Traditional | 11/04/2002SE |
| K946019 | Surgicla Instrument KitFRG · Traditional | 03/20/1995SE |
| K884826 | Gauze SpongeEFQ · Traditional | 12/22/1988SE |
| K810685 | Suture Removal KitGEN · Traditional | 03/26/1981SE |
| K810184 | Laparotomy SpongeGDY · Traditional | 02/04/1981SE |
Questions and answers
When was Burn Dressing cleared by the FDA?
Burn Dressing (K923846) received a 510(k) decision of Substantially Equivalent on September 11, 1992, 42 days after the submission was received.
What is the product code of K923846?
The FDA product code is NAB – Gauze / Sponge,Nonresorbable For External Use, a Class I (low risk) device regulated under 21 CFR 878.4014.