MONOJECT ARTERIAL BLOOD SAMPLING DEVICE— 510(k) K790196

Name: FDA 510(k) clearance K790196
Creator: U.S. Food and Drug Administration
Published: 1979-03-13

Substantially Equivalent

Sherwood Medical Industries

FDA 510(k) clearance K790196 for MONOJECT ARTERIAL BLOOD SAMPLING DEVICE, Substantially Equivalent on 1979-03-13. Applicant: Sherwood Medical Industries. Device class: 1.

Clearance details

Applicant: Sherwood Medical Industries
Product code: Code CBT
Device class: Class 1
Regulation: 21 CFR 868.1100
Advisory panel: Anesthesiology
Date received: 1979-01-25
Decision date: 1979-03-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code CBT

view all

K071269 — HEMODRAW ARTERIAL BLOOD SAMPLING SYSTEM2007-08-01
K070340 — SECURE ARTERIAL BLOOD SAMPLING SYSTEM2007-03-15
K955663 — ABC IN-LINE BLOOD SAMPLING KIT1997-03-17
K954015 — ABG POINT LOK NEEDLE PROTECTION DEVICE1995-11-20
K954035 — ACTI-FLEX ARTERIAL EXTENSION SET1995-09-25

More clearances from Sherwood Medical Industries

view all

K801070 — SHERWOOD DISPOSABLE ENDOMETRIAL SAMPLES1980-07-21
K801071 — LANCER GLUCOSE RATE REAGENT KIT1980-05-23
K792013 — LANCER L-INA HUMAN REFERENCE SERUM1979-11-13
K792014 — LANCER L-INA BUFFER, POLYMER, WASH SOLU1979-11-13
K782077 — LANCER ICE CUBE1979-04-03

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