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510(k) K953622

PTT 6200 ELEVATION THERAPY TABLE by U.S. Table, Inc. — Product Code INQ

K953622 is an FDA 510(k) premarket notification submitted by U.S. Table, Inc. for the device "PTT 6200 ELEVATION THERAPY TABLE". The FDA issued a decision of Substantially Equivalent on September 11, 1995. The device falls under product code INQ (Table, Powered), a Class I device regulated under 21 CFR 890.3760. U.S. Table, Inc. has at least 4 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 11, 1995
Date Received
August 3, 1995
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 U.S. Table, Inc.

  • K953621 — EVT-3300 (November 14, 1995)
  • K951419 — FLEX D-4000 (June 30, 1995)
  • K952600 — EVT-5000BX (June 22, 1995)
  • K951228 — ASH-7000 (May 17, 1995)

Other clearances for product code INQ

  • K960334 — CARDON PHYSICAL THERAPY TABLE MODEL R27116 (February 13, 1996)
  • K960332 — CARDON PHYSICAL THERAPY TABLE MODEL R28598 (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)
  • 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)
  • K952359 — THE HILL ADJUSTABLE HA90C (June 22, 1995)

FDA data resources