Matria Healthcare, Inc.: FDA filings under this applicant name
FDA lists 0 510(k) clearances under the applicant name “Matria Healthcare, Inc.”, plus 3 PMA decisions, across 2 product codes in 1 review panel. Related companies, subsidiaries and acquired businesses that file under other applicant names are counted on their own pages, not here.
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| LQK | Home Uterine Activity Monitor | 2 | 0 |
| HFM | Monitor, Uterine Contraction, External (For Use In Clinic) | 1 | 0 |
Review panels
PMA and De Novo decisions
| Number | Pathway | Device | Decision date |
|---|---|---|---|
| P910063 | PMA | CAREFONE(TM)HOME UTERINE ACTIVITY MONITOR SYSTEM | 1995-09-29 |
| P920038 | PMA | SYSTEM 37 HOME UTERINE ACTIVITY MONITORING SYSTEM | 1995-09-29 |
| P890063 | PMA | GENESIS(R) HOME UTERINE ACTIVITY MONITORING SYSTEM | 1990-09-12 |
Recalls
openFDA lists no recalls under a recalling firm named Matria Healthcare, Inc..
Recalling firms are matched to this applicant name by name only (same normalization), so related entities that recall under another name are not counted. A recall count says nothing about how safe one company's devices are compared with another's.
Frequently asked questions
How many FDA 510(k) clearances are listed under Matria Healthcare, Inc.?
FDA lists 0 510(k) clearances under the applicant name “Matria Healthcare, Inc.”, plus 3 PMA decisions, across 2 product codes in 1 review panel. Filings under other applicant names, such as subsidiaries, are not included.
Which FDA product codes appear under Matria Healthcare, Inc.?
The most frequent FDA product codes under this applicant name are LQK (Home Uterine Activity Monitor, 2); HFM (Monitor, Uterine Contraction, External (For Use In Clinic), 1).
Next steps
- See all 0 Matria Healthcare, Inc. clearances with predicates and recalls
- Run predicate analysis for product code LQK, Matria Healthcare, Inc.'s most frequent
Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Each page covers one FDA applicant name, with punctuation and legal suffixes removed; filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.