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510(k) K802805

NEMECTRODYN 5 by Nemectron Medical, Inc.

K802805 is an FDA 510(k) premarket notification submitted by Nemectron Medical, Inc. for the device "NEMECTRODYN 5". The FDA issued a decision of SESP on November 5, 1980. Nemectron Medical, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESP ()
Decision Date
November 5, 1980
Date Received
November 5, 1980
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by Nemectron Medical, Inc.

  • K923396 — THERMODYN (May 26, 1993)
  • K895000 — NEMECTRON MICROWAVE (July 27, 1990)
  • K862376 — NEMECTROSON MODEL 2 (July 23, 1986)
  • K854720 — NEMECTRODYN MODEL 2 & ENDOVAC 2 POWER MUSCLE STIM. (March 10, 1986)
  • K854721 — NEMECTRODYN MODEL 2 & ENDOVAC 2 (March 6, 1986)
  • K844416 — THERMOPULS E (March 12, 1985)
  • K843734 — NEMDI (October 25, 1984)
  • K843735 — SOFTEPIL (October 25, 1984)
  • K823511 — EMG BIOFEEDBACK DEVICE (March 31, 1983)
  • K820334 — NEMECTRODYN MODELS 8,7,5 (VOLS. I-IV (March 15, 1982)

FDA data resources