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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 Mar 15, 1982. Nemectron Medical, Inc. has 12 other 510(k) clearances on record.

Clearance details

Decision
SESE (Substantially Equivalent)
Decision Date
Mar 15, 1982
Date Received
Feb 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 (Jul 27, 1990)
  • K862376 — NEMECTROSON MODEL 2 (Jul 23, 1986)
  • K854720 — NEMECTRODYN MODEL 2 & ENDOVAC 2 POWER MUSCLE STIM. (Mar 10, 1986)
  • K854721 — NEMECTRODYN MODEL 2 & ENDOVAC 2 (Mar 6, 1986)
  • K844416 — THERMOPULS E (Mar 12, 1985)
  • K843734 — NEMDI (Oct 25, 1984)
  • K843735 — SOFTEPIL (Oct 25, 1984)
  • K823511 — EMG BIOFEEDBACK DEVICE (Mar 31, 1983)
  • K810513 — ELECTRODYN CII-INTERFERENTIAL MUSCLE (May 11, 1981)

FDA data resources

Source: FDA 510(k) database entry for K820334. Report a data issue: hello@regdatalab.com.