Adaptor: Kaps Cine to Moeller Beamsplitter

FDA 510(k) K900160 · Jedmed Instrument Co.

Substantially Equivalent

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)

Official FDA 510(k) record

Device classification

Product code
KQM – Camera, Surgical And Accessories
Device class
Class I (low risk)
Regulation
21 CFR 878.4160
Specialty
General, Plastic Surgery

Other 510(k)s with product code KQM

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K882958Sony Video Printers, Up SeriesKQM · Traditional Sony Medical Electronics Co.08/04/1988SE
K882924Medicam MC-7 and RP-7 Surgical CamerasKQM · Traditional M.P. Video, Inc.07/26/1988SE
K873419Video Printer SystemKQM · Traditional Technology For Imaging, Inc.11/02/1987SE
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K863800Endoscopic Video CameraKQM · Traditional Technology For Imaging, Inc.10/14/1986SE
K860904Video Printer, Model 3200KQM · Traditional Medline Industries, Inc.03/28/1986SE
K850749Concept Video Imaging SystemKQM · Traditional Concept, Inc.05/20/1985SE
K843806VIS-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.