3M Dry Silver Imager
FDA 510(k) K855043 · 3M Company
510(k) numberK855043
Submission
- Device name
- 3M Dry Silver Imager
- Applicant
- 3M Company
Cottae Grove, MN, US - Received
- December 17, 1985
- Decision date
- January 10, 1986
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
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| K083522 | Sony UP-DF750 Digital Film ImagerLMC · Traditional | Sony Electronics, Inc. | 01/09/2009SE |
| K081637 | Laser Imager Drypro Model 873LMC · Special | Konica Minolta Medical & Graphic, Inc. | 07/01/2008SE |
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| K061999 | Dry Laser Imager, Drypro Model 832LMC · Traditional | Konica Minolta Medical & Graphic, Inc. | 08/15/2006SE |
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| K222508 | 3M Comply Hydrogen Peroxide Chemical Indicator 1248JOJ · Traditional | 11/01/2022SE |
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Questions and answers
When was 3M Dry Silver Imager cleared by the FDA?
3M Dry Silver Imager (K855043) received a 510(k) decision of Substantially Equivalent on January 10, 1986, 24 days after the submission was received.
What is the product code of K855043?
The FDA product code is LMC – Camera, Multi Format, Radiological, a Class II (moderate risk) device regulated under 21 CFR 892.2040.