Phoenix Medical Technology, Inc.
Andrews, SC, US
Phoenix Medical Technology, Inc. appears in FDA device records in Andrews, SC. FDA records list 11 510(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
- 11
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 11 510(k) clearances for Phoenix Medical Technology, Inc. between 1986 and 2000. The busiest year on record is 1989, with 5. The most recent is 2000, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1986 | 1 |
| 1989 | 5 |
| 1990 | 2 |
| 1991 | 1 |
| 1995 | 1 |
| 2000 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K000223 | NITRILE PATIENT EXAMINATION GLOVES, POWDER-FREE | LZA | Substantially Equivalent | |
| K945045 | PATIENT EXAINATION GLOVES | LYY | Substantially Equivalent | |
| K905031 | PATIENT EXAMINATION GLOVES | LYZ | Substantially Equivalent | |
| K900454 | MODIFIED LOW POWDER SINGLE USE LATEX EXAM GLOVES | LYY | Substantially Equivalent | |
| K900453 | MODIFIED SINGLE USE LATEX EXAMINATION GLOVES | LYY | Substantially Equivalent | |
| K890917 | PHOENIX DRAPES WITH MICROBAN | KGX | Substantially Equivalent | |
| K892976 | SINGLE USE VINYL EXAM GLOVES - COLOR CODED | LYZ | Substantially Equivalent | |
| K892975 | LOW POWDER SINGLE USE LATEX EXAM GLOVES | LYY | Substantially Equivalent | |
| K891949 | PATIENT EXAMINATION GLOVES (LATEX) | LYY | Substantially Equivalent | |
| K891132 | PATIENT EXAMINATION GLOVE | LYZ | Substantially Equivalent | |
| K853993 | DOBE (MODIFIED) | DRX | 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