EPIDURAL MINIPACK— 510(k) K924541

Unknown

Concord/Portex

FDA 510(k) clearance K924541 for EPIDURAL MINIPACK, Unknown on 1993-07-09. Applicant: Concord/Portex. Device class: 1.

Clearance details

Applicant: Concord/Portex
Product code: Code BYO
Device class: Class 1
Regulation: 21 CFR 868.5220
Advisory panel: Anesthesiology
Date received: 1992-09-08
Decision date: 1993-07-09
Decision: Unknown
Clearance type: Traditional
Location: Keene, NH, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code BYO

K913527 — HYPERFREE1992-01-21
K780558 — BOTTLE BREATHING DEVICE1978-05-26
K780407 — 2C7125 BLOW BOTTLE1978-04-10

More clearances from Concord/Portex

K923559 — STERI-CATH MDI1993-10-25
K930218 — SUBCUTANEOUS TUNNELING NEEDLE AND HANDLES1993-07-27
K930286 — DRI-VENDT/PROVENT/ACCUVENT ARTERIAL BLOOD GAS KITS1993-06-22
K923127 — NEEDLE-PRO CARTRIDGE1993-04-29
K923910 — HEAT MOISTURE CONDENSER1993-01-26

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