Perkinelmer, Xrpad 4336 Med Flat Panel Detector
FDA 510(k) K140551 · Perkinelmer, Inc.
510(k) numberK140551
Submission
- Device name
- Perkinelmer, Xrpad 4336 Med Flat Panel Detector
- Applicant
- Perkinelmer, Inc.
Waltham, MA, US - Received
- March 4, 2014
- Decision date
- August 1, 2014
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
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| K243556 | Lux HD 35 Detector (Lux HD 35); Lux HD 43 Detector (Lux HD 43)MQB · Traditional | Iray Imaging Technology (Haining) Limited | 03/18/2025SE |
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| K161966 | PerkinElmer XRpad2 4336 HWC-M Flat Panel DetectorMQB · Special | 09/08/2016SE |
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| K142698 | PerkinElmer, XRpad 4343 F MED Flat Panel DetectorMQB · Special | 10/23/2014SE |
| K121864 | Perkinelmer 226 Sample Collection DevicesPJC · Abbreviated | 03/12/2013SE |
| K122495 | Perkinelmer XRD 1622 AP3 Med Flat Panel DetectorMQB · Traditional | 11/28/2012SE |
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Questions and answers
When was Perkinelmer, Xrpad 4336 Med Flat Panel Detector cleared by the FDA?
Perkinelmer, Xrpad 4336 Med Flat Panel Detector (K140551) received a 510(k) decision of Substantially Equivalent on August 1, 2014, 150 days after the submission was received.
What is the product code of K140551?
The FDA product code is MQB – Solid State X-Ray Imager (Flat Panel/Digital Imager), a Class II (moderate risk) device regulated under 21 CFR 892.1680.