Evermed, Inc.
Phoenix, AZ, US
Evermed, Inc. appears in FDA device records in Phoenix, AZ. FDA records list 9 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 9
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 9 510(k) clearances for Evermed, Inc. between 1983 and 2002. The busiest year on record is 1983, with 4. The most recent is 2002, with 3.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1983 | 4 |
| 1984 | 2 |
| 2002 | 3 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K023993 | GALAXY SERIES WHEELCHAIR | IOR | Substantially Equivalent | |
| K024030 | MILLENNIUM SERIES MANUAL WHEELCHAIRS | IOR | Substantially Equivalent | |
| K023485 | EXPLORER POWERED WHEELCHAIR | ITI | Substantially Equivalent | |
| K840846 | STERILE HICHMAN/BROVIAC INJECTION CAP | LJS | Substantially Equivalent | |
| K840529 | STEIGER TUNNELING INSTRUMENT 285 | DRC | Substantially Equivalent | |
| K830406 | NON-STERILE CATHETER REPAIR KITS | LJS | Substantially Equivalent | |
| K830256 | NON-STERILE BROVIAC PARENTERAL ALIMI- | LJS | Substantially Equivalent | |
| K830233 | NON-STERILE,SINGLE/SOUBLE LUMEN-CATH | LJS | Substantially Equivalent | |
| K830257 | NON-STERILE PERITONEAL ACCESS CATHET- | FKX | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain