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510k Database
Manufacturers
DE
Zeppelin GmbH
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Medical Device Manufacturer
·
DE , West Germany
Zeppelin GmbH - FDA 510(k) Cleared Devices
2 submissions
·
2 cleared
·
Since 1990
2
Total
2
Cleared
0
Denied
FDA 510(k) Regulatory Record - Zeppelin GmbH
Neurology
✕
2
devices
1-2 of 2
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Cleared
Sep 04, 1990
MAINZ HEAD FIXATION BY PERNECZKY
K901393
·
HBL
Neurology
·
162d
Cleared
Jun 28, 1990
LAMINECTOMY RONGEUR
K901372
·
HAE
Neurology
·
98d
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Neurology
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