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510(k) K041781

VENTILAIR II MEDICAL AIR COMPRESSOR by Hamilton Medical AG — Product Code BTI

K041781 is an FDA 510(k) premarket notification submitted by Hamilton Medical AG for the device "VENTILAIR II MEDICAL AIR COMPRESSOR". The FDA issued a decision of Substantially Equivalent on March 14, 2005. The device falls under product code BTI (Compressor, Air, Portable), a Class II device regulated under 21 CFR 868.6250. Hamilton Medical AG has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 14, 2005
Date Received
July 1, 2004
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 Hamilton Medical AG

  • K201306 — HAMILTON-C3 (February 5, 2021)
  • K201658 — Hamilton-C6 (December 11, 2020)
  • K193228 — Hamilton-G5 (May 4, 2020)
  • K181216 — HAMILTON-T1, HAMILTON-C1 (August 2, 2019)
  • K163283 — HAMILTON-H900, HAMILTON-BC8010, HAMILTON-BC4010 (September 20, 2017)
  • K161450 — HAMILTON-C3 (April 27, 2017)
  • K153046 — HAMILTON-MR1 (September 6, 2016)
  • K152029 — HAMILTON-H900, HAMILTON-BC8022, HAMILTON-BC4022, HAMILTON-BC8010, HAMILTON-BC401 (May 3, 2016)
  • K150893 — IntelliCuff (January 29, 2016)
  • K140939 — HAMILTON-T1,HAMILTON-C1 (September 2, 2015)

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)
  • 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)
  • K031686 — AEROMIST LT, MODEL HCS15004 (January 21, 2004)

FDA data resources