VIEW-LITE, MODEL-DL
FDA 510(k) clearance K802216 · decided 1980-10-23
Clearance details
- K-number
- K802216
- Device name
- VIEW-LITE, MODEL-DL
- Applicant
- Med-Western Electronics, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1980-09-12
- Decision date
- 1980-10-23
- Days to decision
- 41 days
- Clearance type
- Traditional
- Product code
- IXC
- Device class
- 1
- Regulation number
- 892.1890
- Medical specialty
- Radiology
- Advisory committee
- Radiology
- Location
- Mchenry, IL, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| SMARTLIGHT DIGITAL FILM VIEWER, MODELS SL 4000PLUS, SL 2000PLUS (K991302) | Smartlight, Inc. | 1999-06-01 |
| SMART MOTORIZED VIEWER (K973965) | Smartlight, Ltd. | 1997-12-12 |
| ARRIPRO 35 ST/TV (K973115) | Arnold & Richter Cine Technik | 1997-09-02 |
| DIFFUSER PANEL (K970240) | Focused Viewer, Inc. | 1997-03-11 |
| LILY DARK VIEWER (K954998) | Lily Imaging Solutions Co. | 1996-01-29 |
| VOXBOX (K954199) | Voxel | 1995-09-29 |
| ADVIEWER 2000 (K952188) | Adp , Ltd. | 1995-05-30 |
| ULTRALITE X-RAY FILM ILLUMINATOR (K922848) | A & S Trading Co. | 1992-09-28 |
| ROTOLUX, SELECTOLUX, SHUTTERVUE (K922079) | American Medical Sales, Inc. | 1992-06-16 |
| EXCELVIEW ILLUMINATOR (K883702) | Excel Medical Products, Inc. | 1988-09-19 |
| VARIVIEWER (X-RAY FILM VIEWER) (K875233) | Diversified Diagnostic Products, Inc. | 1988-01-19 |
| PROVIEW (E7015) & PROLINK IMAGE DISPLAY SYSTEM (K872245) | General Electric Co. | 1987-06-19 |
Recalls involving this device
No recalls on record reference this clearance.