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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