PNEUMATIC DORSIFLEXOR— 510(k) K890200

Name: FDA 510(k) clearance K890200
Creator: U.S. Food and Drug Administration
Published: 1989-02-03

Substantially Equivalent

Medical Flotation Systems, Inc.

FDA 510(k) clearance K890200 for PNEUMATIC DORSIFLEXOR, Substantially Equivalent on 1989-02-03. Applicant: Medical Flotation Systems, Inc.. Device class: 1.

Clearance details

Applicant: Medical Flotation Systems, Inc.
Product code: Code BXB
Device class: Class 1
Regulation: 21 CFR 890.5380
Advisory panel: Physical Medicine
Date received: 1989-01-18
Decision date: 1989-02-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Herndon, VA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code BXB

view all

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 Medical Flotation Systems, Inc.

view all

K893801 — M.F.S. LOW AIR LOSS PULSATING BED1989-07-25
K884907 — BUMPY MEDICAL MASSAGE MAT1988-12-27
K884908 — ULTRAFLOTATION MEDICAL WHEELCHAIR1988-12-27
K882607 — ULTRAFLOTATION BED1988-10-14

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