FLOW CONTROLLING EXTENSION SET— 510(k) K935236

Name: FDA 510(k) clearance K935236
Creator: U.S. Food and Drug Administration
Published: 1994-02-24

Substantially Equivalent

Block Medical, Inc.

FDA 510(k) clearance K935236 for FLOW CONTROLLING EXTENSION SET, Substantially Equivalent on 1994-02-24. Applicant: Block Medical, Inc.. Device class: 2.

Clearance details

Applicant: Block Medical, Inc.
Product code: Code LDR
Device class: Class 2
Regulation: 21 CFR 880.5725
Advisory panel: General Hospital
Date received: 1993-11-01
Decision date: 1994-02-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Carlsbad, 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 Block Medical, Inc.

view all

K944692 — C-SERIES HOMEPUMP1995-05-02
K940117 — MID-5001994-06-10
K934551 — VERIFUSE AMBULATORY PUMP1994-03-17
K932740 — HOMEPUMP NSF1993-10-06
K904663 — AUTO SASH (TM)1992-11-23

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