Fresenius Hemocare, Inc.: FDA filings under this applicant name
FDA lists 0 510(k) clearances under the applicant name “Fresenius Hemocare, Inc.”, plus 1 PMA decision, across 1 product code 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 |
|---|---|---|---|
| MDP | Separator For Therapeutic Purposes, Membrane Automated Blood Cell/Plasma | 1 | 0 |
Review panels
PMA and De Novo decisions
| Number | Pathway | Device | Decision date |
|---|---|---|---|
| P850020 | PMA | PROSORBA(TM) COLUMN | 1987-12-23 |
Recalls
2 product recalls in 2 recall events; 0 initiated in the last five years. Most recent: 2003-07-11.
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.
Other FDA applicant names starting with the same word
FDA records these as separate applicants. Some may belong to the same corporate group and some may not; their filings are not included in the counts above.
- Fresenius Medical Care Renal Therapies Group, LLC (52 510(k)s)
- Fresenius Medical Care North America (42 510(k)s)
- Fresenius USA, Inc. (38 510(k)s)
- Fresenius Kabi AG (12 510(k)s)
- Fresenius Medical Care (7 510(k)s)
- Fresenius Medical Care North America, Design Cente (5 510(k)s)
- Fresenius Hemotechnology, Inc. (3 510(k)s)
- Fresenius Pharma (3 510(k)s)
- Fresenius AG (2 510(k)s)
- Fresenius Kabi (2 510(k)s)
- Fresenius Kabi USA,Llc (2 510(k)s)
- Fresenius Medical Care South Asia Pacific Pty , Ltd. (2 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Fresenius Hemocare, Inc.?
FDA lists 0 510(k) clearances under the applicant name “Fresenius Hemocare, Inc.”, plus 1 PMA decision, across 1 product code in 1 review panel. Filings under other applicant names, such as subsidiaries, are not included.
Which FDA product codes appear under Fresenius Hemocare, Inc.?
The most frequent FDA product codes under this applicant name are MDP (Separator For Therapeutic Purposes, Membrane Automated Blood Cell/Plasma, 1).
Next steps
- See all 0 Fresenius Hemocare, Inc. clearances with predicates and recalls
- Run predicate analysis for product code MDP, Fresenius Hemocare, 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.