Specboard Jr.
FDA 510(k) K123414 · Macbrud Corp., Medical Division
510(k) numberK123414
Submission
- Device name
- Specboard Jr.
- Applicant
- Macbrud Corp., Medical Division
Miami, FL, US - Received
- November 6, 2012
- Decision date
- January 11, 2013
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Other 510(k)s with product code IZH
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K203509 | Smart FinderIZH · Special | Ims Giotto S.P.A. | 07/14/2021SE |
| K202294 | Affirm Contrast BiopsyIZH · Special | Hologic, Inc. | 10/05/2020SE |
| K191495 | Biopsy PositionerIZH · Special | Fujifilm Corporation | 07/03/2019SE |
| K161575 | Affirm Lateral Arm Upright Biopsy AccessoryIZH · Traditional | Hologic | 08/10/2016SE |
| K161920 | Comfort CoverIZH · Traditional | Precision Dynamics Corporation | 07/15/2016SE |
| K153486 | Affirm Prone Biopsy SystemIZH · Traditional | Hologic, Inc. | 04/01/2016SE |
| K152038 | MammoGRIPIZH · Traditional | Women'S Imaging Solutions Enterprises, LLC | 12/22/2015SE |
| K122836 | Affirm Breast Biopsy Guidance SystemIZH · Special | Lorad, A Hologic Co. | 01/11/2013SE |
| K113607 | Biopsy Digit S Biopsy SLIZH · Traditional | Giotto USA, LLC | 08/10/2012SE |
| K113284 | Biopsy PositionerIZH · Traditional | Fuji Film Medical Systems | 03/07/2012SE |
Questions and answers
When was Specboard Jr. cleared by the FDA?
Specboard Jr. (K123414) received a 510(k) decision of Substantially Equivalent on January 11, 2013, 66 days after the submission was received.
What is the product code of K123414?
The FDA product code is IZH – System, X-Ray, Mammographic, a Class II (moderate risk) device regulated under 21 CFR 892.1710.