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510(k) K892649

VERIMED MYOEXORCISER III (MYO III) by Verimed Holdings, Inc. — Product Code HCC

K892649 is an FDA 510(k) premarket notification submitted by Verimed Holdings, Inc. for the device "VERIMED MYOEXORCISER III (MYO III)". The FDA issued a decision of Substantially Equivalent on December 13, 1989. The device falls under product code HCC (Device, Biofeedback), a Class II device regulated under 21 CFR 882.5050. Verimed Holdings, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 13, 1989
Date Received
April 12, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Device, Biofeedback
Device Class
Class II
Regulation Number
882.5050
Review Panel
NE
Submission Type

Other clearances by Verimed Holdings, Inc.

  • K981277 — PERIFORM (November 20, 1998)
  • K954127 — BIOFEEDBACK DEVICE (November 14, 1995)
  • K951969 — MYOEXORCISER II FUAL (June 14, 1995)
  • K930670 — PHYACTION 787 (July 2, 1993)
  • K922550 — ROMAS (RANGE OF MOTION ASSESSMENT SYSTEM) (December 10, 1992)
  • K913912 — VERIMED PERINEOMETER (June 16, 1992)
  • K893220 — VERIMED MYOEXORCISER VERISTIM (March 7, 1990)
  • K874212 — VERIMED MYO/PREMS (August 8, 1988)
  • K854193 — ELECTRO-MYOGRAPHIC PERINEOMETER (June 9, 1986)
  • K852963 — MYO-ACTUATOR (January 21, 1986)

Other clearances for product code HCC

  • K233580 — A Breathing System (ABS) (August 1, 2024)
  • K222101 — Prism (March 17, 2023)
  • K180173 — Freespira (August 23, 2018)
  • K163448 — GrindCare System (September 1, 2017)
  • K151050 — Pacifier Activated Lullaby (PAL®) (December 22, 2015)
  • K143507 — NFANT Feeding Solution (September 9, 2015)
  • K131586 — CANARY BREATHING SYSTEM (December 10, 2013)
  • K122879 — EEGER4 MODEL 4.3 (February 6, 2013)
  • K111687 — EMG SYSTEM (September 29, 2011)
  • K092675 — GRINDCARE (March 3, 2010)

FDA data resources