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510(k) K930692

LATHAM TABLE by I-Rep, Inc. — Product Code INQ

K930692 is an FDA 510(k) premarket notification submitted by I-Rep, Inc. for the device "LATHAM TABLE". The FDA issued a decision of Substantially Equivalent on February 2, 1994. The device falls under product code INQ (Table, Powered), a Class I device regulated under 21 CFR 890.3760. I-Rep, Inc. has at least 7 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 2, 1994
Date Received
February 10, 1993
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 I-Rep, Inc.

  • K930691 — ACCUTRAC TRACTION UNIT (July 22, 1993)
  • K861864 — MEDTRON TYPE P-300 ULTRASONIC THERAPY UNIT (July 14, 1986)
  • K854947 — REHABILITATION TABLES (January 3, 1986)
  • K851690 — ADJUSTABLE TREATMENT TABLES (May 7, 1985)
  • K842268 — VACUPULSE VACUUM UNIT (July 20, 1984)
  • K832940 — ROTAGYM (November 7, 1983)
  • K822906 — PHYSICAL MEDICINE & REHABILITATION EQUIP (October 15, 1982)

Other clearances for product code INQ

  • K960334 — CARDON PHYSICAL THERAPY TABLE MODEL R27116 (February 13, 1996)
  • K960336 — CARDON PHYSICAL THERAPY TABLE MODEL R27645 (February 13, 1996)
  • K960332 — CARDON PHYSICAL THERAPY TABLE MODEL R28598 (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)
  • K951955 — CARDON PHYSICAL THERAPY TABLE MODEL:R40194 (June 22, 1995)

FDA data resources