LIDO(R) LINEA— 510(k) K924513

Substantially Equivalent

Loredan Biomedical, Inc.

FDA 510(k) clearance K924513 for LIDO(R) LINEA, Substantially Equivalent on 1993-03-31. Applicant: Loredan Biomedical, Inc.. Device class: 1.

Clearance details

Applicant: Loredan Biomedical, Inc.
Product code: Code BXB
Device class: Class 1
Regulation: 21 CFR 890.5380
Advisory panel: Physical Medicine
Date received: 1992-09-04
Decision date: 1993-03-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: West Sacramento, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code BXB

K072887 — G-TRAINER MEDICAL2008-01-25
K003272 — FLO-BOOT2001-04-04
K952975 — ANKLE CALF EXERCISER PHLEBOPUMP1996-09-25
K953456 — E-Z FLEX1996-01-26
K955105 — BTE CPM-101995-12-29

More clearances from Loredan Biomedical, Inc.

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