Atlas FDA

VIEW-LITE, MODEL-S

FDA 510(k) clearance K802215 · decided 1980-10-23

Clearance details

K-number
K802215
Device name
VIEW-LITE, MODEL-S
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.

RecordFirmDate
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 Technik1997-09-02
DIFFUSER PANEL (K970240)Focused Viewer, Inc.1997-03-11
LILY DARK VIEWER (K954998)Lily Imaging Solutions Co.1996-01-29
VOXBOX (K954199)Voxel1995-09-29
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.