Medical Device Manufacturer · US , San Diego , CA

Applinc - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1985
2
Total
2
Cleared
0
Denied

Applinc has 2 FDA 510(k) cleared medical devices. Based in San Diego, US.

Historical record: 2 cleared submissions from 1985 to 1985. Primary specialty: Anesthesiology.

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

FDA 510(k) Regulatory Record - Applinc

2 devices
1-2 of 2
Cleared May 15, 1985
ADDITION OF 50% OXYGEN TO APPLINC SAVING BREATH HY
K851245 · BZE
Anesthesiology · 49d
Cleared Jan 16, 1985
RESPIRATORY GAS HUMIDIFIER
K842597 · BZE
Anesthesiology · 197d
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