MASTER FLOW I.V. PUMPETTE— 510(k) K905497

Name: FDA 510(k) clearance K905497
Creator: U.S. Food and Drug Administration
Published: 1991-04-16

Substantially Equivalent

The Master Medical Corp.

FDA 510(k) clearance K905497 for MASTER FLOW I.V. PUMPETTE, Substantially Equivalent on 1991-04-16. Applicant: The Master Medical Corp.. Device class: 2.

Clearance details

Applicant: The Master Medical Corp.
Product code: Code LDR
Device class: Class 2
Regulation: 21 CFR 880.5725
Advisory panel: General Hospital
Date received: 1990-12-07
Decision date: 1991-04-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Francisco, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LDR

view all

K242693 — DEKA Infusion System, DEKA Administration Set2024-10-07
K232316 — DEKA Infusion System, DEKA Administration Set2024-03-01
K153760 — Volumetric Infusion Controller2016-10-03
K963136 — PACER MODEL 100 INFUSION CONTROLLER1997-10-10
K971826 — ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER M12/5001997-07-03

More clearances from The Master Medical Corp.

view all

K913076 — I.V. INSTANT TIMER1991-10-17
K905498 — STAT 2 IV PUMPETTE1991-04-16
K871753 — MASTER MEDICAL DEVICE IS I.V. STAT 21987-06-05
K852254 — I.V. STAT MASTER1985-11-18
K792560 — MASTER I.V. DIAL LOCK1979-12-20

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