Worldheart, Inc.: FDA clearances and approvals
Worldheart, Inc. has 0 FDA 510(k) clearances, plus 1 PMA decision, across 1 product code in 1 review panel.
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| DSQ | Ventricular (Assist) Bypass | 1 | 0 |
Review panels
- Cardiovascular (1)
PMA and De Novo decisions
| Number | Pathway | Device | Decision date |
|---|---|---|---|
| P980012 | PMA | NOVACOR LVAS | 1998-09-29 |
Recalls
openFDA lists no recalls under a recalling firm named Worldheart, Inc..
Recalling firms are matched to this company by name only (same normalization as the applicant), so related entities that recall under another name are not counted.
Frequently asked questions
How many FDA 510(k) clearances does Worldheart, Inc. have?
Worldheart, Inc. has 0 FDA 510(k) clearances, plus 1 PMA decision, across 1 product code in 1 review panel.
What devices does Worldheart, Inc. make?
Its most frequent FDA product codes are DSQ (Ventricular (Assist) Bypass, 1).
Has Worldheart, Inc. had device recalls?
openFDA lists no recalls under a recalling firm name matching Worldheart, Inc. Related entities may recall under other names.
Next steps
- See all 0 Worldheart, Inc. clearances with predicates and recalls
- Run predicate analysis for product code DSQ, Worldheart, Inc.'s most frequent
Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Companies are grouped by FDA applicant name with punctuation and legal suffixes removed. Review days run from FDA receipt to decision. Not regulatory advice.