Medical Device Manufacturer · US , Sunnyvale , CA

Charlton Assoc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1994
2
Total
2
Cleared
0
Denied

Charlton Assoc. has 2 FDA 510(k) cleared medical devices. Based in Sunnyvale, US.

Historical record: 2 cleared submissions from 1994 to 1995. Primary specialty: Chemistry.

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

FDA 510(k) Regulatory Record - Charlton Assoc.

2 devices
1-2 of 2
Cleared Apr 20, 1995
BIONIKE A/Q PREGNANCY TEST
K951136 · JHI
Chemistry · 38d
Cleared Jul 06, 1994
BODYWISE PREGNANCEY TEST
K941771 · LCX
Chemistry · 86d
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