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510(k) K820079

AIRMED PNEUMATIC EQUIP. FILTRA/CONTROL by James L. Geraci & Associates, Inc. — Product Code BTI

K820079 is an FDA 510(k) premarket notification submitted by James L. Geraci & Associates, Inc. for the device "AIRMED PNEUMATIC EQUIP. FILTRA/CONTROL". The FDA issued a decision of Substantially Equivalent on February 5, 1982. The device falls under product code BTI (Compressor, Air, Portable), a Class II device regulated under 21 CFR 868.6250. James L. Geraci & Associates, Inc. has at least 4 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 5, 1982
Date Received
January 12, 1982
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 James L. Geraci & Associates, Inc.

  • K853927 — LASE SYSTEM II (October 16, 1985)
  • K820091 — AIRMED SMOKE EVACUATION & FILTER (February 24, 1982)
  • K820078 — DRAPE, SURGICAL (February 4, 1982)
  • K811698 — CARL ZEISS INN MYRINGOTOMY TUBE LINE (August 31, 1981)

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