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510(k) K924905

MEDI-PLINTH by Medi-Man Rehabilitation Products, Inc. — Product Code INQ

K924905 is an FDA 510(k) premarket notification submitted by Medi-Man Rehabilitation Products, Inc. for the device "MEDI-PLINTH". The FDA issued a decision of Substantially Equivalent on February 16, 1993. The device falls under product code INQ (Table, Powered), a Class I device regulated under 21 CFR 890.3760. Medi-Man Rehabilitation Products, Inc. has at least 3 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 16, 1993
Date Received
September 29, 1992
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Table, Powered
Device Class
Class I
Regulation Number
890.3760
Review Panel
PM
Submission Type

Other clearances by Medi-Man Rehabilitation Products, Inc.

  • K992779 — A-2000 BATHING SYSTEMS; HYDROSONIC BATHIN SYSTEM (January 13, 2000)
  • K925195 — MALIBU BATHING SYSTEM (October 17, 1994)
  • K844976 — MEDI-MAN WATER POWERED BATH LIFT & HYDRAULIC LIFT (April 1, 1985)

Other clearances for product code INQ

  • K960332 — CARDON PHYSICAL THERAPY TABLE MODEL R28598 (February 13, 1996)
  • K960334 — CARDON PHYSICAL THERAPY TABLE MODEL R27116 (February 13, 1996)
  • K960336 — CARDON PHYSICAL THERAPY TABLE MODEL R27645 (February 13, 1996)
  • K960196 — TRI W-G, INC TABLE, TILT/EXAM/TREATMENT MODEL 777 (February 7, 1996)
  • K953621 — EVT-3300 (November 14, 1995)
  • K953622 — PTT 6200 ELEVATION THERAPY TABLE (September 11, 1995)
  • K952357 — THE HILL ADJUSTABLE PODIATRY MODEL (July 6, 1995)
  • K951419 — FLEX D-4000 (June 30, 1995)
  • K952358 — THE HILL ADJUSTABLE P.T. MOBILIZATION TABLE (June 22, 1995)
  • K952356 — THE HILL ADJUSTABLE COUNTERSTRAIN TABLE (June 22, 1995)

FDA data resources