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510(k) K854194

IMT ULTRASONIC STRIDE MONITOR by Innovative Medical Technologies, Inc.

K854194 is an FDA 510(k) premarket notification submitted by Innovative Medical Technologies, Inc. for the device "IMT ULTRASONIC STRIDE MONITOR". The FDA issued a decision of Substantially Equivalent on May 2, 1986. Innovative Medical Technologies, Inc. has at least 5 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 2, 1986
Date Received
October 15, 1985
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by Innovative Medical Technologies, Inc.

  • K220458 — UltraFlo-R Push Button Blood Collection Set (September 29, 2023)
  • K123987 — IMPROVE BLOOD COLLECTION SET AND IMPROSAFE BLOOD COLLECTION SET (August 27, 2013)
  • K972969 — QUICK-DRAW CAPILLARY WHOLE BLOOD COLLECTION SYSTEM (September 22, 1997)
  • K936087 — CARPAL BOX (October 20, 1994)
  • K904237 — RAPID IMMOBILIZATION DEVICE OR R.I.D. SYSTEM (May 9, 1991)

FDA data resources