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510(k) K963349

DEVILBISS 8650D by Devilbiss Health Care, Inc. — Product Code BTI

K963349 is an FDA 510(k) premarket notification submitted by Devilbiss Health Care, Inc. for the device "DEVILBISS 8650D". The FDA issued a decision of Substantially Equivalent on June 13, 1997. The device falls under product code BTI (Compressor, Air, Portable), a Class II device regulated under 21 CFR 868.6250. Devilbiss Health Care, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 13, 1997
Date Received
August 26, 1996
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Compressor, Air, Portable
Device Class
Class II
Regulation Number
868.6250
Review Panel
AN
Submission Type

Other clearances by Devilbiss Health Care, Inc.

  • K970289 — COMPRESSOR/NEBULIZER #3650 (April 15, 1997)
  • K961126 — PULSE DOSE SERIES (October 21, 1996)
  • K950849 — MODEL #7354 (February 8, 1996)
  • K952491 — MODEL 7355 (January 31, 1996)
  • K952249 — JET NEBULIZER (January 30, 1996)
  • K953815 — 5 LPM OXYGEN CONCENTRATOR (November 9, 1995)
  • K952037 — 3 LPM OXYGEN CONCENTRATOR (September 6, 1995)
  • K946095 — DEVILBISS MODEL 5500 (August 24, 1995)
  • K944611 — MODEL# 7500 SURVEYOR (April 21, 1995)
  • K935979 — CONTINUOUS POSITIVE AIRWAY PRESSURE CPAP SYSTEM (November 10, 1994)

Other clearances for product code BTI

  • K131881 — OMBRA TABLE TOP COMPRESSOR (October 24, 2013)
  • K113338 — MEDICAL AIR COMPRESSOR (August 10, 2012)
  • K091871 — DK50 DS (October 23, 2009)
  • K072634 — EMG TRITON -COMP,MODEL NCA01-XXX SERIES (November 19, 2008)
  • K060781 — MEDICAL COMPRESSOR, MODELS DK50 D AND DM (October 3, 2006)
  • K051691 — MINIMATE COMPRESSOR (December 9, 2005)
  • K041781 — VENTILAIR II MEDICAL AIR COMPRESSOR (March 14, 2005)
  • K041406 — NEWPORT C250 AIR COMPRESSOR MODEL C250 (December 15, 2004)
  • K041974 — MED2000 NEBULIZER COMPRESSOR, MODELS P3, P4, P5 WITH NEBULIZER (August 24, 2004)
  • K040220 — MEDICAL AIR COMPRESSOR (June 9, 2004)

FDA data resources