Phoenix Medical Technology, Inc.
Phoenix Medical Technology, Inc. holds FDA 510(k) medical device clearances, first cleared 1986, most recent 2000.
Top product codes for Phoenix Medical Technology, Inc.
Recent clearances by Phoenix Medical Technology, Inc.
- K000223 — NITRILE PATIENT EXAMINATION GLOVES, POWDER-FREE
- K945045 — PATIENT EXAINATION GLOVES
- K905031 — PATIENT EXAMINATION GLOVES
- K900453 — MODIFIED SINGLE USE LATEX EXAMINATION GLOVES
- K900454 — MODIFIED LOW POWDER SINGLE USE LATEX EXAM GLOVES
- K890917 — PHOENIX DRAPES WITH MICROBAN
- K892976 — SINGLE USE VINYL EXAM GLOVES - COLOR CODED
- K892975 — LOW POWDER SINGLE USE LATEX EXAM GLOVES
- K891949 — PATIENT EXAMINATION GLOVES (LATEX)
- K891132 — PATIENT EXAMINATION GLOVE
- K853993 — DOBE (MODIFIED)
Data sourced from openFDA. This site is unofficial and independent of the FDA.