MANUAL AND MOTORIZED FLEXION DISTRACTION TABLES— 510(k) K904950

Name: FDA 510(k) clearance K904950
Creator: U.S. Food and Drug Administration
Published: 1990-11-26

Substantially Equivalent

Leander Research, Mfg & Distr., Inc.

FDA 510(k) clearance K904950 for MANUAL AND MOTORIZED FLEXION DISTRACTION TABLES, Substantially Equivalent on 1990-11-26. Applicant: Leander Research, Mfg & Distr., Inc.. Device class: 1.

Clearance details

Applicant: Leander Research, Mfg & Distr., Inc.
Product code: Code INQ
Device class: Class 1
Regulation: 21 CFR 890.3760
Advisory panel: Physical Medicine
Date received: 1990-11-02
Decision date: 1990-11-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Port Orchard, WA, US

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Recent devices under product code INQ

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K960332 — CARDON PHYSICAL THERAPY TABLE MODEL R285981996-02-13
K960334 — CARDON PHYSICAL THERAPY TABLE MODEL R271161996-02-13
K960336 — CARDON PHYSICAL THERAPY TABLE MODEL R276451996-02-13
K960196 — TRI W-G, INC TABLE, TILT/EXAM/TREATMENT MODEL 7771996-02-07
K953621 — EVT-33001995-11-14

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