Medical Device Manufacturer · US , Walker , MI

Vitacomm, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1984
2
Total
2
Cleared
0
Denied

Vitacomm, Inc. has 2 FDA 510(k) cleared medical devices. Based in Walker, US.

Historical record: 2 cleared submissions from 1984 to 1989. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Vitacomm, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Vitacomm, Inc.
2 devices
1-2 of 2
Cleared Jan 30, 1989
VITACOMM MODEL #140/141 ESOPHAGEAL STETHOSCOPE
K885347 · BZT
Anesthesiology · 33d
Cleared Jun 22, 1984
VITACOMM 100 ESOPHAGEAL STETHOSCOPE
K842309 · BZT
Anesthesiology · 10d
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