BETAFLO 2000 PIGGYBACK SYSTEM— 510(k) K864789

Substantially Equivalent

Betaflo, Inc.

FDA 510(k) clearance K864789 for BETAFLO 2000 PIGGYBACK SYSTEM, Substantially Equivalent on 1987-02-04. Applicant: Betaflo, Inc.. Device class: 2.

Clearance details

Applicant: Betaflo, Inc.
Product code: Code LDR
Device class: Class 2
Regulation: 21 CFR 880.5725
Advisory panel: General Hospital
Date received: 1986-12-08
Decision date: 1987-02-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Menlo Park, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LDR

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 Betaflo, Inc.

K862273 — BETAFLO 20001986-07-18

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