10 results
10-K
2018 Q4
GH
Guardant Health Inc
19 Mar 19
Annual report
5:26pm
510(k)-cleared device, the FDA can require the manufacturer to cease marketing and/or recall the modified device until 510(k) clearance or approval … ;
recall requirements, including a mandatory recall if there is a reasonable probability that the device would cause serious adverse health consequences
10-Q
mq8texeiimm62
19 Nov 18
Quarterly report
12:00am
424B4
c1ggcg ilwkbfbmy
5 Oct 18
Prospectus supplement with pricing info
12:00am
DRS/A
gbfkz d05
13 Aug 18
Draft registration statement (amended)
12:00am
DRS
ypzcfjm0
5 Jul 18
Draft registration statement
12:00am
- Prev
- 1
- Next