11 results
10-K
2021 FY
HLTHQ
Cue Health Inc
29 Mar 22
Annual report
5:17pm
of the modified product at any time and may require the manufacturer to cease marketing and recall the modified device until 510(k) marketing clearance or PMA … reporting regulations; product correction, and recall regulations; and post-market surveillance activities.
Advertising and promotion of medical devices
10-Q
2021 Q3
HLTHQ
Cue Health Inc
10 Nov 21
Quarterly report
5:18pm
on our business, financial condition and results of operations and adversely affect our prospects.
Our products may be subject to recalls. A recall of our … products, could have a significant adverse impact on us.
The FDA has the authority to require the recall of commercialized products that are subject
424B4
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27 Sep 21
Prospectus supplement with pricing info
12:00am
S-1/A
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15 Sep 21
IPO registration (amended)
5:25pm
S-1
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1 Sep 21
IPO registration
5:02pm
DRS/A
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16 Jun 21
Draft registration statement (amended)
12:00am
DRS/A
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24 May 21
Draft registration statement (amended)
12:00am
DRS
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19 Apr 21
Draft registration statement
12:00am
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