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510(k) K761092

INGUINAL COMPRESSIVE DEVICE (ICD) by Medical Electronic Devices, Inc.

K761092 is an FDA 510(k) premarket notification submitted by Medical Electronic Devices, Inc. for the device "INGUINAL COMPRESSIVE DEVICE (ICD)". The FDA issued a decision of Substantially Equivalent on December 16, 1976. Medical Electronic Devices, Inc. has at least 6 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 16, 1976
Date Received
November 22, 1976
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by Medical Electronic Devices, Inc.

  • K052563 — INOGEN SATELLITE CONSERVER, MODEL SC-100 (October 24, 2005)
  • K033197 — INOGEN SATELLITE CONSERVER (May 13, 2004)
  • K023420 — PULSED OXYGEN CONSERVING DEVICE - EVERY BREATH, POCDEB, REACTEB (October 25, 2002)
  • K983601 — DEMAND OXYGEN CONSERVING DEVICE, DOCD, THE DOC (December 15, 1998)
  • K983459 — PULSED OXYGEN CONSERVING DEVICE, POCD (December 8, 1998)
  • K770115 — ARTERIAL DIAGNOSTIC UNIT (ADU) (February 1, 1977)

FDA data resources