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510(k) K770608

WALKING AID by Will Ross Co. — Product Code ITJ

K770608 is an FDA 510(k) premarket notification submitted by Will Ross Co. for the device "WALKING AID". The FDA issued a decision of Substantially Equivalent on April 8, 1977. The device falls under product code ITJ (Walker, Mechanical), a Class I device regulated under 21 CFR 890.3825. Will Ross Co. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 8, 1977
Date Received
March 31, 1977
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Walker, Mechanical
Device Class
Class I
Regulation Number
890.3825
Review Panel
PM
Submission Type

Other clearances by Will Ross Co.

  • K780850 — SEARLE NEONATAL OXYGEN PROBE (August 23, 1978)
  • K771561 — DOVER URINE METER (September 7, 1977)
  • K771132 — KENWOOD BIOLOGICAL STEOILIZ. INDICATOR (July 14, 1977)
  • K770607 — TRACTION HARNESS (April 8, 1977)
  • K770612 — SPLINT, BOHLER (April 8, 1977)
  • K770609 — TABLE, MASSAGE & TREATMHNT, FIXED HEIGHT (April 8, 1977)
  • K770610 — TABLE, TREATMENT & TRACTION, HI-LO (April 8, 1977)
  • K770611 — PARALLEL BARS (April 8, 1977)
  • K770509 — TABLE, MASSAGE AND TREATMENT (April 5, 1977)
  • K770399 — VALVE FOR CLOSED SYS. URINARY DRAINAGE (March 9, 1977)

Other clearances for product code ITJ

  • K833869 — CHILD'S WALKER (November 29, 1983)
  • K833195 — UMBRELLA WALKER (October 27, 1983)
  • K830784 — WALK N ROLL (May 25, 1983)
  • K830848 — RESI-WALKER (April 5, 1983)
  • K823105 — RESI-WALKER (November 5, 1982)
  • K821404 — LIGHT WEIGHT ALUMINUM WALKER (May 21, 1982)
  • K820711 — WALK-A-CYCLE (April 8, 1982)
  • K811485 — WALKER/CRUTCH BAG (June 16, 1981)
  • K792064 — DELTA ROLLING SELF-LICKING WALKER (October 30, 1979)
  • K790529 — WALKING AID (April 3, 1979)

FDA data resources