Diatek, Inc.
Diatek, Inc. holds FDA 510(k) medical device clearances, first cleared 1979, most recent 2002.
Top product codes for Diatek, Inc.
Recent clearances by Diatek, Inc.
- K020430 — DIATEK CONNECTOR ASSEMBLY REPLACEMENT KIT (CARK)
- K010399 — DIATEK CANNON-CATH #CC2400, CC2800, CC3200, CC3600,CC5500. CC2400PC, CC2800PC, CC3200PC(32 CM), CC3200PC(36 CM)
- K895703 — DIATEK MODEL 700 THERMOMETER
- K872178 — MODIFICATION TO ARKIVE(TM)
- K862085 — ARKIVE (TM)
- K841827 — ENTEROPORT NUTRITION PUMP
- K841859 — SECURA SET
- K833568 — DIATEK 600 THERMOMETER SYSTEM
- K830565 — SECURA SET SECONDARY ADMIN. SET
- K830355 — SECURA IV VOLUMETRIC INFUSION PUMP
- K830377 — SECURA SET PRIMARY ADMIN. SET
- K830448 — SECURA SET VOLUME LIMITING SET
- K813468 — ACC-U-THERM TEMPERATURE MONITOR
- K810575 — MARTIN TRACH-SECURE
- K790416 — DIATEK 500
Data sourced from openFDA. This site is unofficial and independent of the FDA.