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510(k) K820334

NEMECTRODYN MODELS 8,7,5 (VOLS. I-IV by Nemectron Medical, Inc.

K820334 is an FDA 510(k) premarket notification submitted by Nemectron Medical, Inc. for the device "NEMECTRODYN MODELS 8,7,5 (VOLS. I-IV". The FDA issued a decision of Substantially Equivalent on March 15, 1982. Nemectron Medical, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 15, 1982
Date Received
February 5, 1982
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)
  • K810513 — ELECTRODYN CII-INTERFERENTIAL MUSCLE (May 11, 1981)

FDA data resources