Model SSD-119
FDA 510(k) K827284 · Aloka Co., Ltd.
510(k) numberK827284
Submission
- Device name
- Model SSD-119
- Applicant
- Aloka Co., Ltd.
Walker, MI, US - Received
- March 30, 1982
- Decision date
- April 21, 1982
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
No product code recorded.
More from Aloka Co., Ltd.
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|---|---|---|
| K111227 | Aloka SSD-3500 Diagnostic Ultrasound SystemIYN · Traditional | 05/13/2011SE |
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| K093488 | Aloka Prosound Alpha 6 Diagnostic Ultrasound SystemIYO · Traditional | 11/20/2009SE |
| K083254 | Aloka Prousound 2 Diagnostic Ultrasound SystemIYN · Traditional | 12/19/2008SE |
| K081843 | Ultrasound Data Analysis System, Model DAS-RS1LLZ · Traditional | 07/15/2008SE |
| K080176 | Aloka Prosound 6 Diagnostic Ultrasound SystemIYN · Traditional | 02/29/2008SE |
| K072285 | Aloka Ssd-Alpha 7 Ultrasound SystemITX · Traditional | 08/30/2007SE |
| K060059 | Aloka SD-3500 Ultrasound SystemIYN · Traditional | 01/13/2006SE |
| K043196 | Aloka Ssd-Alpha 10 Ultrasound SystemIYN · Traditional | 11/30/2004SE |
| K040719 | Aloka Model SSD-4000 Diagnostic Ultrasound System W/Optional Sonoreal 3D System AccessoryIYO · Traditional | 03/26/2004SE |
Questions and answers
When was Model SSD-119 cleared by the FDA?
Model SSD-119 (K827284) received a 510(k) decision of Substantially Equivalent on April 21, 1982, 22 days after the submission was received.