OB HELP ARM— 510(k) K823152

Substantially Equivalent

Orthion Corp.

FDA 510(k) clearance K823152 for OB HELP ARM, Substantially Equivalent on 1982-11-05. Applicant: Orthion Corp.. Device class: 1.

Clearance details

Applicant: Orthion Corp.
Product code: Code ILE
Device class: Class 1
Regulation: 21 CFR 890.3475
Advisory panel: Physical Medicine
Date received: 1982-10-20
Decision date: 1982-11-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code ILE

K830842 — OB HELP ARM1983-04-05
K823811 — OVERHEAD ARM SLINGS1983-01-14

More clearances from Orthion Corp.

K832546 — MARK V HIGH VOLTAGE GALVANIC STIMULATORR1983-10-14
K823105 — RESI-WALKER1982-11-05
K823149 — OB TILT TABLE1982-11-05
K823150 — SESAM TREATMENT TABLE1982-11-05
K823151 — OB TRIPP TRANSPORT CHAIR1982-11-05

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