Product code MWP— Radiology
10 X 10 VISION
- Classification name
- Cabinet, X-Ray System
- Device class
- Class 2
- Regulation
- 21 CFR 892.1680
- Advisory panel
- Radiology
- Total cleared
- 27
- First cleared
- Most recent
Market context for product code MWP
FDA has cleared devices under product code MWP between 1985 and 2023, filed by 12 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.
Clearances per year
last 15 years- 2023
- 2021
- 2020
- 2019
- 2018
- 2017
- 2016
- 2012
- 2011
- 2010
- 2009
- 2008
- 2007
- 2006
- 2005
Top applicants under product code MWP
Recent clearances under product code MWP
- K230136 — TrueView 200 Pro-US Specimen Radiography System (TrueView 200 Pro-US)
- K230140 — TrueView Core 100Pro-US Core Specimen Radiography System (TrueView Core 100Pro-US)
- K213691 — Solas OR
- K210955 — Kubtec Mozart Supra (XPERT 84) Radiography System
- K210956 — Kubtec Mozart (XPERT42)
- K210957 — Kubec Xpert 80 Radiography System
- K202713 — TrueView 100 Pro
- K200756 — Kubtec Mozart Supra
- K192939 — Volumetric Specimen Imager
- K193317 — CoreLite X-Ray Specimen Cabinet
- K183624 — Kubtec Mozart (Xpert42)
- K183142 — PathVisionXL
- K182727 — Trident HD Specimen Radiography System
- K173309 — Faxitron VisionCT
- K170786 — Faxitron Bioptics Speciemen Radiography System
- K153583 — BioVision Plus
- K122428 — FAXITRON SPECIEN RADIOGRAPHY SYSTEM
- K111508 — TRIDENT SPECIMEN RADIOGRAPHY SYSTEM, MODEL : RC TRI-00001
- K091928 — 10 X 10 VISION
- K091558 — BIOVISION DIGITAL SPECIMEN RADIOGRAPHY SYSTEM
- K082432 — CORE VISION DIGITAL SPECIMEN RADIOGRAPHY (DSR) SYSTEM
- K072557 — FAXITRON SPECIMEN RADIOGRAPHY SYSTEM, MODEL MX-20
- K071233 — XPERT 40 SPECIMEN RADIOGRAPHY SYSTEM
- K061361 — FAXITRON DIGITAL RADIOGRAPHY SYSTEM, MODEL DX-50
- K052433 — PIXARRAY 100 DIGITAL SPECIMEN RADIOGRAPHY (DSR) SYSTEM
- K021113 — MAMMOPATH
- K852634 — MICRO-FOCUS 50 CABINET X-RAY
Data sourced from openFDA. This site is unofficial and independent of the FDA.