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510(k) K850740

SECHRIST VOLUME VENTILATOR MODIFICATION by Sechrist Industries, Inc.

K850740 is an FDA 510(k) premarket notification submitted by Sechrist Industries, Inc. for the device "SECHRIST VOLUME VENTILATOR MODIFICATION". The FDA issued a decision of Substantially Equivalent on July 29, 1985. Sechrist Industries, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 29, 1985
Date Received
January 28, 1985
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by Sechrist Industries, Inc.

  • K140559 — SECHRIST MONOPLACE HYPERBARIC OXYGEN CHAMBER (May 30, 2014)
  • K100268 — SECHRIST MONOPLACE HYPERBARIC OXYGEN CHAMBER (April 26, 2010)
  • K052713 — MODEL 3300E/ER MONOPLACE HYPERBARIC OXYGEN CHAMBER (October 28, 2005)
  • K023745 — SECHRIST AIR/OXYGEN MIXER, MODEL 3500 CP-G (January 17, 2003)
  • K993167 — MILLENNIUM INFANT VENTILATOR (November 10, 1999)
  • K992503 — SECHRIST AIR-OXYGEN MIXER, 3500/3500HL SERIES (August 10, 1999)
  • K950386 — MODEL 3200P/3200PR HYPERBARIC CHAMBER (June 13, 1995)
  • K934164 — MODEL 2500E/2500ER HYPERBARIC CHAMBER (June 13, 1995)
  • K930713 — THE INFANT FLOW SYSTEM (September 16, 1993)
  • K914607 — SEHRIST VOLUME VENTILATOR, MODEL 2200B (November 2, 1992)

FDA data resources