FDA 510(k) Applications Submitted by GUILIN WOODPECKER MEDICAL INSTRUMENT CO., LTD

FDA 510(k) Number Submission Date Device Name Applicant
K080025 01/04/2008 LED.L, LED.M, LED.G, LED.B GUILIN WOODPECKER MEDICAL INSTRUMENT CO., LTD
K111290 05/06/2011 PIEZO BONE SURGERY GUILIN WOODPECKER MEDICAL INSTRUMENT CO., LTD
K053555 12/20/2005 ULTRASONIC SCALER, MODELS UDS-N1, UDS-N2. UDS-J, UDS-K, UDS-L GUILIN WOODPECKER MEDICAL INSTRUMENT CO., LTD


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