Medical Device Manufacturer · US , Mchenry , IL

American Bentley - FDA 510(k) Cleared Devices

59 submissions · 59 cleared · Since 1983
59
Total
59
Cleared
0
Denied
FDA 510(k) Regulatory Record - American Bentley General & Plastic Surgery ✕
2 devices
1-2 of 2
Cleared Mar 09, 1987
ELECTROSURGICAL MENISCUS CUTTER (EMC) MOD. AMC-100
K870269 · GEI
General & Plastic Surgery · 45d
Cleared Aug 12, 1985
ELECTROSURGICAL LATERAL RELEASE PROBE MOD ALR-100
K852683 · GEI
General & Plastic Surgery · 48d
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All59 Cardiovascular 50 Anesthesiology 4 Gastroenterology & Urology 2 General & Plastic Surgery 2 Hematology 1