Hanaulux(R) 2000
FDA 510(k) K895715 · W.C. Heraeus GmbH
510(k) numberK895715
Submission
- Device name
- Hanaulux(R) 2000
- Applicant
- W.C. Heraeus GmbH
West Germany, DE - Received
- September 25, 1989
- Decision date
- October 13, 1989
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- FTD – Lamp, Surgical
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 878.4580
- Specialty
- General, Plastic Surgery
Other 510(k)s with product code FTD
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K133425 | Scintillant Dual Bent Tip Surgical Light, Scintillant Dual Straight Tip Surgical LightFTD · Special | Engineered Medical Solutions Co., LLC | 12/05/2013SE |
| K130513 | Volista 400; Volista 600FTD · Special | Maquet S.A.S. | 05/08/2013SE |
| K123776 | Polaris 100/200FTD · Abbreviated | Drager Medical GmbH | 03/08/2013SE |
| K111020 | Atricure DissectorFTD · Special | AtriCure, Inc. | 06/09/2011SE |
| K100234 | Hm-Lamp IIFTD · Traditional | Hillusa, Inc. | 07/08/2010SE |
| K100884 | Stryker KnifelightFTD · Traditional | Howmedica Osteonics Corp. | 06/25/2010SE |
| K071180 | Scintillant Surgical Light, Model 2644-01-0001FTD · Traditional | Engineered Medical Solutions Co., LLC | 06/20/2007SE |
| K053364 | Halux Iris Examination and Surgical LampFTD · Traditional | Waldmann Lighting | 02/23/2006SE |
| K041681 | Atricure DissectorFTD · Traditional | AtriCure, Inc. | 07/01/2004SE |
| K013242 | Amsco Harmony Surgical Lighting and Media SystemFTD · Abbreviated | STERIS Corporation | 12/13/2001SE |
More from STERIS Corporation
| 510(k) | Device | Decision |
|---|---|---|
| K875078 | Heracure LS 500HHR · Traditional | 02/22/1988SE |
Questions and answers
When was Hanaulux(R) 2000 cleared by the FDA?
Hanaulux(R) 2000 (K895715) received a 510(k) decision of Substantially Equivalent on October 13, 1989, 18 days after the submission was received.
What is the product code of K895715?
The FDA product code is FTD – Lamp, Surgical, a Class II (moderate risk) device regulated under 21 CFR 878.4580.