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510(k) K915846

BIODEX SYSTEM 2 AUTOPROGRAM by Biodex Corp. — Product Code IKK

K915846 is an FDA 510(k) premarket notification submitted by Biodex Corp. for the device "BIODEX SYSTEM 2 AUTOPROGRAM". The FDA issued a decision of Substantially Equivalent on January 13, 1992. The device falls under product code IKK (System, Isokinetic Testing And Evaluation), a Class II device regulated under 21 CFR 890.1925. Biodex Corp. has at least 6 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 13, 1992
Date Received
December 13, 1991
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, Isokinetic Testing And Evaluation
Device Class
Class II
Regulation Number
890.1925
Review Panel
PM
Submission Type

Other clearances by Biodex Corp.

  • K915648 — BIODEX SYSTEM 2 AUTOPROGRAM (January 9, 1992)
  • K913021 — BIODEX,MODEL B-2000 (October 3, 1991)
  • K913020 — BIODEX SYSTEM 2,MODEL S2-S (October 3, 1991)
  • K900450 — BIODEX LIFT SIMULATOR (July 24, 1990)
  • K900741 — BIODEX BACK SYSTEM ATTACHMENT (February 26, 1990)
  • K860821 — BIODEX SYSTEM (April 18, 1986)

Other clearances for product code IKK

  • K123746 — AMES THERAPY DEVICE (May 24, 2013)
  • K952090 — HUMAC SYSTEM (December 11, 1995)
  • K951770 — BIODEX SYSTEM 3 MODEL S3S-AP AND MODEL S3D-3AP (November 16, 1995)
  • K951916 — CC RIDER, MODEL ME180 (October 4, 1995)
  • K950095 — CYBEX 770 (June 21, 1995)
  • K942229 — MOTIVATOR FTR 2000 (February 27, 1995)
  • K944732 — DEXTER ISOKINETIC (February 3, 1995)
  • K924414 — THE BTE DYNAMIC LIFT (February 12, 1993)
  • K923350 — CLOSED CHAIN ATTACHMENT, MODEL #820-520 (July 23, 1992)
  • K922772 — TWO POSITION ROLL-UP BACK ATTACHMENT CHAIR (July 13, 1992)

FDA data resources