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510(k) K851690

ADJUSTABLE TREATMENT TABLES by I-Rep, Inc.

K851690 is an FDA 510(k) premarket notification submitted by I-Rep, Inc. for the device "ADJUSTABLE TREATMENT TABLES". The FDA issued a decision of Substantially Equivalent on May 7, 1985. I-Rep, Inc. has at least 7 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 7, 1985
Date Received
April 16, 1985
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by I-Rep, Inc.

  • K930692 — LATHAM TABLE (February 2, 1994)
  • K930691 — ACCUTRAC TRACTION UNIT (July 22, 1993)
  • K861864 — MEDTRON TYPE P-300 ULTRASONIC THERAPY UNIT (July 14, 1986)
  • K854947 — REHABILITATION TABLES (January 3, 1986)
  • K842268 — VACUPULSE VACUUM UNIT (July 20, 1984)
  • K832940 — ROTAGYM (November 7, 1983)
  • K822906 — PHYSICAL MEDICINE & REHABILITATION EQUIP (October 15, 1982)

FDA data resources