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510(k) K841569

MAXI-MISER HUMIDIFIER INSERT 1020 by Nova-Ventrx

K841569 is an FDA 510(k) premarket notification submitted by Nova-Ventrx for the device "MAXI-MISER HUMIDIFIER INSERT 1020". The FDA issued a decision of Substantially Equivalent on May 30, 1984. Nova-Ventrx has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 30, 1984
Date Received
April 17, 1984
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by Nova-Ventrx

  • K952267 — CRITERION, CRITERION I.V., MODIFIED (December 2, 1997)
  • K954480 — CONDENSATE COLLECTION KIT (December 29, 1995)
  • K893760 — CRITERION I.V. VENTILATOR BREATHING CIRCUIT #1004 (August 10, 1989)
  • K881207 — RES-Q 1, 2, 3, 4 AND 5 (August 15, 1988)
  • K870382 — DRV DISP RESUSCIT 3000/BAG ADAPT 3010 & 3011 (March 6, 1987)
  • K863756 — MODIFIED CRITERION VENTILATOR BREATHING CIRCUIT (November 13, 1986)
  • K850600 — CO-AX VENTILATOR CIRCUIT (May 2, 1985)
  • K842794 — MAXI-MISER HUMIDIFIER INSERT 1020 & 1021 (October 4, 1984)
  • K842795 — MAXI-MISER HUMIDIFIER INSERT 1030 (October 4, 1984)
  • K841571 — MAXI-MISER WATER TRANSFER SET 1021/1022 (May 30, 1984)

FDA data resources