Hook Scissor
FDA 510(k) K854896 · Euro-Med Intl.
510(k) numberK854896
Submission
- Device name
- Hook Scissor
- Applicant
- Euro-Med Intl.
Danville, CA, US - Received
- December 6, 1985
- Decision date
- May 2, 1986
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- KDC – Instrument, Surgical, Disposable
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 878.4800
- Specialty
- General, Plastic Surgery
Other 510(k)s with product code KDC
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K943229 | Disposable Surgical Scissors and ForcepsKDC · Traditional | Y.M.K. International Co., Ltd. | 08/19/1994SE |
| K936226 | Surgimed Breast Localization Needle Wire SetKDC · Traditional | Meadox Medicals, Div. Boston Scientific Corp. | 03/07/1994SE |
| K920153 | Thermuff BagKDC · Traditional | Techstyles | 07/01/1992SE |
| K920263 | Manual Surgical InstrumentsKDC · Traditional | Phoenix Instruments Div. | 05/06/1992SE |
| K915064 | Disposable Cautery Abrasive PadKDC · Traditional | American Medical Mfg., Inc. | 03/11/1992SE |
| K914960 | Instrument OrganizerKDC · Traditional | O.R. Concepts, Inc. | 02/28/1992SE |
| K912834 | Shur-GripKDC · Traditional | Inman Medical Corp. | 07/26/1991SE |
| K910079 | Disposable Introducer SheathKDC · Traditional | Applied Vascular Devices, Inc. | 02/27/1991SE |
| K905240 | VesseloopsKDC · Traditional | Sparta Surgical Corp. | 02/06/1991SE |
| K903649 | Bradley Tenaculum HolderKDC · Traditional | Marlo Surgical Technology | 11/02/1990SE |
More from Marlo Surgical Technology
| 510(k) | Device | Decision |
|---|---|---|
| K883884 | Prostatic Core-Cut NeedleKNW · Traditional | 12/05/1988SE |
| K882404 | Kevor-CurettePCF · Traditional | 07/08/1988SE |
| K854901 | Pacific GrasperKDC · Traditional | 05/02/1986SE |
| K854898 | Atlantic GrasperKDC · Traditional | 05/02/1986SE |
| K854897 | Max-I-GraspKDC · Traditional | 05/02/1986SE |
| K854895 | Basket ForcepKDC · Traditional | 05/02/1986SE |
| K854894 | SpoonKDC · Traditional | 05/02/1986SE |
| K854891 | KnifeEMF · Traditional | 05/02/1986SE |
| K854890 | Hook ProbeKDC · Traditional | 05/02/1986SE |
| K854889 | Flex-I-GraspHRX · Traditional | 02/21/1986SE |
Questions and answers
When was Hook Scissor cleared by the FDA?
Hook Scissor (K854896) received a 510(k) decision of Substantially Equivalent on May 2, 1986, 147 days after the submission was received.
What is the product code of K854896?
The FDA product code is KDC – Instrument, Surgical, Disposable, a Class I (low risk) device regulated under 21 CFR 878.4800.