Sony WBS-700H Videocassette Recorder System
FDA 510(k) K902535 · Sony Medical Electronics Co.
510(k) numberK902535
Submission
- Device name
- Sony WBS-700H Videocassette Recorder System
- Applicant
- Sony Medical Electronics Co.
North Attleboro, MA, US - Received
- June 8, 1990
- Decision date
- June 29, 1990
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
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| K980279 | Sony DXC-LS1 Color Video CameraGCJ · Traditional | 04/24/1998SE |
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| K904447 | Sony Cine Video System SME-3500IZI · Traditional | 10/17/1990SE |
| K901153 | Sony VO-5800H Videocassette RecorderJAA · Traditional | 04/19/1990SE |
| K885042 | Sony Trinitron Color Video Monitor PVM-1343MDKQM · Traditional | 12/22/1988SE |
| K884008 | Sony Cine Video System SME-3300IZI · Traditional | 11/30/1988SE |
| K882958 | Sony Video Printers, Up SeriesKQM · Traditional | 08/04/1988SE |
Questions and answers
When was Sony WBS-700H Videocassette Recorder System cleared by the FDA?
Sony WBS-700H Videocassette Recorder System (K902535) received a 510(k) decision of Substantially Equivalent on June 29, 1990, 21 days after the submission was received.
What is the product code of K902535?
The FDA product code is JAA – System, X-Ray, Fluoroscopic, Image-Intensified, a Class II (moderate risk) device regulated under 21 CFR 892.1650.