Adaptor: Kaps Cine to Moeller Beamsplitter
FDA 510(k) K900160 · Jedmed Instrument Co.
510(k) numberK900160
Submission
- Device name
- Adaptor: Kaps Cine to Moeller Beamsplitter
- Applicant
- Jedmed Instrument Co.
St. Louis, MO, US - Received
- January 12, 1990
- Decision date
- January 24, 1990
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- KQM – Camera, Surgical And Accessories
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 878.4160
- Specialty
- General, Plastic Surgery
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|---|---|---|---|
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| K882958 | Sony Video Printers, Up SeriesKQM · Traditional | Sony Medical Electronics Co. | 08/04/1988SE |
| K882924 | Medicam MC-7 and RP-7 Surgical CamerasKQM · Traditional | M.P. Video, Inc. | 07/26/1988SE |
| K873419 | Video Printer SystemKQM · Traditional | Technology For Imaging, Inc. | 11/02/1987SE |
| K871595 | Surgical Camera AccessoriesKQM · Traditional | M.P. Video, Inc. | 05/07/1987SE |
| K863800 | Endoscopic Video CameraKQM · Traditional | Technology For Imaging, Inc. | 10/14/1986SE |
| K860904 | Video Printer, Model 3200KQM · Traditional | Medline Industries, Inc. | 03/28/1986SE |
| K850749 | Concept Video Imaging SystemKQM · Traditional | Concept, Inc. | 05/20/1985SE |
| K843806 | VIS-1000 Video SystemKQM · Traditional | Vistek Corp. | 12/12/1984SE |
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Questions and answers
When was Adaptor: Kaps Cine to Moeller Beamsplitter cleared by the FDA?
Adaptor: Kaps Cine to Moeller Beamsplitter (K900160) received a 510(k) decision of Substantially Equivalent on January 24, 1990, 12 days after the submission was received.
What is the product code of K900160?
The FDA product code is KQM – Camera, Surgical And Accessories, a Class I (low risk) device regulated under 21 CFR 878.4160.