Angiomed Skin Fascia Knife
FDA 510(k) K855104 · Angiomed U.S., Inc.
510(k) numberK855104
Submission
- Device name
- Angiomed Skin Fascia Knife
- Applicant
- Angiomed U.S., Inc.
Anaheim, CA, US - Received
- December 23, 1985
- Decision date
- January 24, 1986
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- GES – Blade, Scalpel
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 878.4800
- Specialty
- General, Plastic Surgery
Other 510(k)s with product code GES
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K032242 | Personna Plus Safety Scalpel SystemGES · Traditional | Omi Manufacturing Pty., Ltd. | 09/23/2003SE |
| K932998 | Easy-OnGES · Traditional | Devon Industries, Inc. | 08/18/1993SE |
| K923170 | Los Alamos Retractable KnifeGES · Traditional | Innovative Surgical Technology, Inc. | 02/18/1993SE |
| K915119 | Scalpel Blade Remover (Bladegard)GES · Traditional | Intergrated Visual, Inc. | 05/05/1992SE |
| K911913 | Precision Glide - Enhanced Surgical BladeGES · Traditional | Bd Becton Dickinson Vacutainer Systems Preanalytic | 05/13/1991SE |
| K900266 | Sterile Carbon Steel Surgical BladeGES · Traditional | Rahn Laboratories | 03/01/1990SE |
| K884862 | Anchor Double-Edge Myringotomy BladeGES · Traditional | Anchor Products Co. | 12/27/1988SE |
| K881638 | Surgical BladeGES · Traditional | Far East Intl. Trading Corp. | 06/15/1988SE |
| K880244 | Surgical BladesGES · Traditional | Ailee C/O Havel'S, Inc. | 02/10/1988SE |
| K873493 | Ninja ScalpelGES · Traditional | Primrose Medical, Inc. | 09/24/1987SE |
More from Primrose Medical, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K874771 | Angiomed Introducing SetsDWB · Traditional | 01/12/1988SE |
| K874585 | Angiomed Osty-Cut Bone Biopsy NeedleDWO · Traditional | 12/02/1987SE |
| K864225 | Angiomed Ureteral D&M Sets/Ureteroscopy Guid StentFAD · Traditional | 01/30/1987SE |
| K863386 | Vesico Suprapubic Bladder Drainage & Exchange SetsKOB · Traditional | 10/24/1986SE |
| K862805 | Angiomed Vac-U-Cut Biopsy NeedleGDM · Traditional | 09/29/1986SE |
| K863446 | Angiomed High Pressure ConnectorsGCD · Traditional | 09/23/1986SE |
| K854910 | AngioflowDQO · Traditional | 07/17/1986SE |
| K854912 | Angiomed Guied WiresDQX · Traditional | 04/16/1986SE |
| K854908 | UroflexFAD · Traditional | 03/14/1986SE |
| K855143 | Angiomed Exchange Drainage Catheter SetsKOD · Traditional | 03/11/1986SE |
Questions and answers
When was Angiomed Skin Fascia Knife cleared by the FDA?
Angiomed Skin Fascia Knife (K855104) received a 510(k) decision of Substantially Equivalent on January 24, 1986, 32 days after the submission was received.
What is the product code of K855104?
The FDA product code is GES – Blade, Scalpel, a Class I (low risk) device regulated under 21 CFR 878.4800.