ACCU-VENT(TM) WITH NEEDLE-PRO(TM)— 510(k) K912043

Unknown

Concord/Portex

FDA 510(k) clearance K912043 for ACCU-VENT(TM) WITH NEEDLE-PRO(TM), Unknown on 1991-07-05. Applicant: Concord/Portex. Device class: 1.

Clearance details

Applicant: Concord/Portex
Product code: Code CBT
Device class: Class 1
Regulation: 21 CFR 868.1100
Advisory panel: Anesthesiology
Date received: 1991-05-08
Decision date: 1991-07-05
Decision: Unknown
Clearance type: Traditional
Location: Keene, NH, US

Download summary PDF View on FDA.gov ↗

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K955663 — ABC IN-LINE BLOOD SAMPLING KIT1997-03-17
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K954035 — ACTI-FLEX ARTERIAL EXTENSION SET1995-09-25

More clearances from Concord/Portex

K923559 — STERI-CATH MDI1993-10-25
K930218 — SUBCUTANEOUS TUNNELING NEEDLE AND HANDLES1993-07-27
K924541 — EPIDURAL MINIPACK1993-07-09
K930286 — DRI-VENDT/PROVENT/ACCUVENT ARTERIAL BLOOD GAS KITS1993-06-22
K923127 — NEEDLE-PRO CARTRIDGE1993-04-29

Data sourced from openFDA. This site is unofficial and independent of the FDA.