Raney Clip
FDA 510(k) K884783 · Alto Development Corp.
510(k) numberK884783
Submission
- Device name
- Raney Clip
- Applicant
- Alto Development Corp.
Farmingdale, NJ, US - Received
- November 15, 1988
- Decision date
- November 30, 1988
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- FZQ – Clip, Removable (Skin)
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 878.4320
- Specialty
- General, Plastic Surgery
Other 510(k)s with product code FZQ
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K873744 | Leukoclip(R)FZQ · Traditional | Beiersdorf, Inc. | 09/30/1987SE |
| K830768 | Disposable Skin StaplerFZQ · Traditional | Surgeons Choice, Inc. | 04/12/1983SE |
| K830704 | One Time Disposable Skin StaplerFZQ · Traditional | Acme United Corp. | 04/12/1983SE |
| K822963 | Surgical Products, Skin Staple RemoverFZQ · Traditional | Temp-Stik Corp. | 11/08/1982SE |
| K822145 | CompleteFZQ · Traditional | Richard-Allan Medical Ind., Inc. | 10/22/1982SE |
More from Richard-Allan Medical Ind., Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K964621 | A & E Medical Electrocautery Suction Tube with Finger Tip Activator ButtonGEI · Traditional | 12/20/1996SE |
| K932513 | Labeling for Myo/Wire II Sternotomy SuturesGAO · Traditional | 01/07/1994SE |
| K931537 | A&E Medical Electrosurg Electro W/Non-Stick CoatGEI · Traditional | 09/07/1993SE |
| K930528 | A&E Medical Electrosurgical Connecting CordsGEI · Traditional | 05/17/1993SE |
| K914193 | A&E Medical Corp Dispos Suct Coag W/Non Stick CoatGEI · Traditional | 10/05/1992SE |
| K915300 | A & Em Medical Electrosurgical Pencil/AccessoriesGEI · Traditional | 02/18/1992SE |
| K881413 | Electro-Cautery Suction TubeGEI · Traditional | 04/21/1988SE |
| K831867 | Pressure Monitoring IV Bottle CapDRS · Traditional | 08/12/1983SE |
| K821518 | Myo/ClipLDF · Traditional | 07/08/1982SE |
Questions and answers
When was Raney Clip cleared by the FDA?
Raney Clip (K884783) received a 510(k) decision of Substantially Equivalent on November 30, 1988, 15 days after the submission was received.
What is the product code of K884783?
The FDA product code is FZQ – Clip, Removable (Skin), a Class I (low risk) device regulated under 21 CFR 878.4320.