Video Print
FDA 510(k) K840385 · Advanced Instruments, Inc.
510(k) numberK840385
Submission
- Device name
- Video Print
- Applicant
- Advanced Instruments, Inc.
- Received
- January 30, 1984
- Decision date
- February 27, 1984
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
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Questions and answers
When was Video Print cleared by the FDA?
Video Print (K840385) received a 510(k) decision of Substantially Equivalent on February 27, 1984, 28 days after the submission was received.
What is the product code of K840385?
The FDA product code is LMC – Camera, Multi Format, Radiological, a Class II (moderate risk) device regulated under 21 CFR 892.2040.