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510(k) K812179

LIFE-TECH #1753 BIOFEEDBACK TRAINER by Life-Tech Instruments, Inc. — Product Code HCC

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 25, 1981
Date Received
August 3, 1981
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 Life-Tech Instruments, Inc.

  • K812177 — LIFE-TECH #1857 PRESSURE/POLOT MODULE (September 9, 1981)
  • K812180 — LIFE-TECH #5102 VISULAB (August 21, 1981)
  • K812178 — LIFE-TECH #'S 1106/1156 UROLABS (August 13, 1981)
  • K800112 — AMBLYOPIA TRAINER (March 10, 1980)
  • K790663 — MODEL 1750 STANDING URINAL (April 24, 1979)
  • K790664 — MODEL 1309 AUDIO MONITOR (April 23, 1979)
  • K781476 — MULAR GOLD LEAF ELECTRODE MODEL 7501 (November 15, 1978)
  • K781461 — MODEL 7320 VISUAL STIMULATOR (November 8, 1978)
  • K781474 — PREAMPLIFIER MODELS 8101PI & 8102PI (September 7, 1978)
  • K781475 — ELECTRODE IMPEDANCE TESTER-MODEL 500 (September 7, 1978)

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