UNIFLEX— 510(k) K830316

Substantially Equivalent

Buckman Consultants

FDA 510(k) clearance K830316 for UNIFLEX, Substantially Equivalent on 1983-03-24. Applicant: Buckman Consultants. Device class: 1.

Clearance details

Applicant: Buckman Consultants
Product code: Code BXB
Device class: Class 1
Regulation: 21 CFR 890.5380
Advisory panel: Physical Medicine
Date received: 1983-01-31
Decision date: 1983-03-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, 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 Buckman Consultants

K823882 — M-BRACE1983-01-17
K821829 — UROGARD1982-07-30

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