SINGLE CHAIR INTEGRAL BACK ATTACHMENT— 510(k) K922092

Name: FDA 510(k) clearance K922092
Creator: U.S. Food and Drug Administration
Published: 1992-05-26

Substantially Equivalent

Biodan Medical Systems, Ltd.

FDA 510(k) clearance K922092 for SINGLE CHAIR INTEGRAL BACK ATTACHMENT, Substantially Equivalent on 1992-05-26. Applicant: Biodan Medical Systems, Ltd.. Device class: 2.

Clearance details

Applicant: Biodan Medical Systems, Ltd.
Product code: Code IKK
Device class: Class 2
Regulation: 21 CFR 890.1925
Advisory panel: Physical Medicine
Date received: 1992-05-05
Decision date: 1992-05-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shirley, NY, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code IKK

view all

K123746 — AMES THERAPY DEVICE2013-05-24
K952090 — HUMAC SYSTEM1995-12-11
K951770 — BIODEX SYSTEM 3 MODEL S3S-AP AND MODEL S3D-3AP1995-11-16
K951916 — CC RIDER, MODEL ME1801995-10-04
K950095 — CYBEX 7701995-06-21

More clearances from Biodan Medical Systems, Ltd.

view all

K932153 — THYROID UPTAKE SYSTEM & ATOMLAB 950 MED. SPECTROME1993-09-07
K930261 — RTM REHABILITATION TREADMILL, MODEL #945-2001993-05-26
K930262 — TREATMENT TABLE, MODEL #825-1001993-03-29
K930259 — TRACTION TABLE MODEL #825-2001993-03-24
K926083 — NUCLEAR PATIENT SANNING TABLES, VARIOUS TYPES1993-02-12

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