MIDLAND THREE SECTION P.T. TABLE W/ DRAINAGE— 510(k) K924002

Name: FDA 510(k) clearance K924002
Creator: U.S. Food and Drug Administration
Published: 1992-11-09

Substantially Equivalent

Midland Mfg. Co.

FDA 510(k) clearance K924002 for MIDLAND THREE SECTION P.T. TABLE W/ DRAINAGE, Substantially Equivalent on 1992-11-09. Applicant: Midland Mfg. Co.. Device class: 1.

Clearance details

Applicant: Midland Mfg. Co.
Product code: Code INQ
Device class: Class 1
Regulation: 21 CFR 890.3760
Advisory panel: Physical Medicine
Date received: 1992-08-10
Decision date: 1992-11-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Great Neck, NY, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code INQ

view all

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

More clearances from Midland Mfg. Co.

view all

K933311 — MOTORIZED ELECTRIC PARALLEL BARS1994-01-26
K925164 — ELECTRIC STAND-IN TABLE1993-03-24
K924093 — ELECTRIC HI LO TILT TABLE1993-02-12
K923973 — SPACE BASE ELECTRIC TILT TABLE1992-11-09
K923998 — MIDLAND TILT TABLE1992-11-09

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