Gibeck, Inc.
Gibeck, Inc. holds FDA 510(k) medical device clearances, first cleared 1990, most recent 1997.
Top product codes for Gibeck, Inc.
Recent clearances by Gibeck, Inc.
- K965016 — ISO-GARD FILTER ANGLED(18212)/ISO-GARD FILTER STRAIGHT(19212)
- K964377 — THERMAL REGULATION SYSTEM BLANKET
- K964382 — HUMID-VENT FILTER COMPACT ANGLED (18402)/HUMID-VENT FILTER COMPACT STRAIGHT(19402)
- K960511 — GIBECK WARMBAG REUSABLE CONVECTIVE WARMING BLANKET
- K954828 — ISO-GARD HEPA FILTER-HME, ISO-ARD HEPA FILTER-HME W/PORT
- K953491 — HUMID-VENT 1 PORT/HUMID-VENT 1 PORT ANGLE
- K953544 — HUMID-VENT 2 LIGHT/HUMID-VENT 2 PORT LIGHT
- K952845 — HUMID-VENT TRACH-VENT
- K952750 — HUMID-VENT 1
- K952844 — HUMID-VENT 2
- K952084 — HUMID-VENT FILTER PEDI
- K951856 — HUMID-VENT MICRO
- K914747 — XENON CIRCUIT
- K900979 — GAS SAMPLING NASAL CANNULA
- K897171 — DISPOSABLE CO2 ABSORBER/E
Data sourced from openFDA. This site is unofficial and independent of the FDA.