Intercept-Urethral Microcoil
FDA 510(k) K011781 · Surgi-Vision, Inc.
510(k) numberK011781
Submission
- Device name
- Intercept-Urethral Microcoil
- Applicant
- Surgi-Vision, Inc.
Gaithersburg, MD, US - Received
- June 7, 2001
- Decision date
- August 31, 2001
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Other 510(k)s with product code MOS
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K262330 | dS Breast 7ch 1.5TdS Breast 7ch 3.0TdS Breast 16ch 1.5TdS Breast 16ch 3.0TdS Breast Coil…MOS · Special | Philips Medical Systems Nederland B.V. | 07/30/2026SE |
| K262294 | dS FootAnkle 16Ch 1.5T;dS FootAnkle 16Ch 3.0T;dS HiRes Hand/Wrist 16Ch 1.5T;dS HiRes…MOS · Special | Philips Medical Systems Nederland B.V. | 07/24/2026SE |
| K260947 | 0.55T 12Ch Breast CoilMOS · Special | Neocoil, LLC | 04/23/2026SE |
| K252587 | HD 8Ch Wrist ArrayMOS · Traditional | Shenzhen RF Tech Co., Ltd. | 04/14/2026SE |
| K252876 | GEM Flex Coil 16-L Array, 3.0T Receive Only; GEM Flex Coil 16-M Array, 3.0T Receive…MOS · Traditional | Shenzhen RF Tech Co., Ltd. | 04/01/2026SE |
| K260519 | Smart Fit TorsoCardiac 1.5TMOS · Special | Philips Healthcare (Suzhou) Co., Ltd. | 03/20/2026SE |
| K252179 | GEM Flex Coil 16-L Array, 1.5T Receive Only; GEM Flex Coil 16-M Array, 1.5T Receive…MOS · Traditional | Shenzhen RF Tech Co., Ltd. | 02/10/2026SE |
| K253738 | 3.0T Air 32CH HnaMOS · Abbreviated | Ge Healthcare Coils (Usa Instruments, Inc.) | 01/23/2026SE |
| K254190 | dS Base 1.5T; dS Base 3.0T; dS Head 1.5T; dS Head 3.0T; dS HeadNeck 1.5T; dS HeadNeck 3.0TMOS · Special | Philips Medical Systems Nederland B.V. | 01/14/2026SE |
| K253182 | InkSpace Imaging Small Body Array (SBA12PH30x)MOS · Special | Inkspace Imaging, Inc. | 10/20/2025SE |
More from Inkspace Imaging, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K111073 | Surgivision Inc. Clearpoint SystemORR · Traditional | 06/22/2011SE |
| K020790 | Intercept Esophageal Internal MR Coil, Intercept Urethral Microcoil, and Intercept…MOS · Traditional | 05/21/2002SE |
| K020495 | Intercept Esophageal Internal MR Coil, Intercept Urethral Internal MR Coil, and…MOS · Traditional | 04/23/2002SE |
| K003436 | Surgi-Vision Guidewire CoilMOS · Traditional | 02/02/2001SE |
| K002916 | Surgi-Vision Prostate CoilMOS · Traditional | 11/28/2000SE |
| K002345 | Surgi-Vision Urethral CoilMOS · Traditional | 10/11/2000SE |
| K994436 | Surgi-Vision Esophageal Stylet CoilMOS · Traditional | 03/14/2000SE |
| K992193 | Endo-Esophageal MR CoilMOS · Traditional | 09/03/1999SE |
Questions and answers
When was Intercept-Urethral Microcoil cleared by the FDA?
Intercept-Urethral Microcoil (K011781) received a 510(k) decision of Substantially Equivalent on August 31, 2001, 85 days after the submission was received.
What is the product code of K011781?
The FDA product code is MOS – Coil, Magnetic Resonance, Specialty, a Class II (moderate risk) device regulated under 21 CFR 892.1000.