Home / 510(k) Clearances / K903489

510(k) K903489

THERA-MIST TM VOLUMINA INCENT SPIROMETER, P40000 by Pegasus Research Corp. — Product Code BWF

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 10, 1990
Date Received
August 2, 1990
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Spirometer, Therapeutic (Incentive)
Device Class
Class II
Regulation Number
868.5690
Review Panel
AN
Submission Type

Other clearances by Pegasus Research Corp.

  • K122857 — HOPE CONTINUOUS NEBULIZER MODEL HOPE-11310, HEART NEBULIZER MODEL HEART-100609, (November 7, 2012)
  • K020700 — PMH 5000 HEATED HUMIDIFIER FOR RESPIRATORY THERAPY (April 26, 2004)
  • K013856 — PMH 1000 HEATED HUMIDIFIER (February 21, 2003)
  • K983783 — HEATED HUMIDIFIER (October 24, 2000)
  • K962534 — THERA-MIST NEBULIZER MODEL-P3000 (February 28, 1997)
  • K946057 — AQUALARM MOISTURE SENSOR MODEL P85000 (May 5, 1995)
  • K915890 — AUTOCLAVABLE THERA-MIST HUMIDIFIER P3600, MODIFIED (June 24, 1992)
  • K914465 — AUTOCLAVABLE VERSION THERA-MIST NEBULIZER, P32000 (March 31, 1992)
  • K893942 — THERA-MIST(TM) NEBULIZER, MODEL 30000 (August 28, 1989)
  • K894000 — THERA-MIST HUMIDIFIER (August 28, 1989)

Other clearances for product code BWF

  • K241152 — InSee (August 21, 2025)
  • K233855 — AllPEP (February 2, 2024)
  • K221058 — LungTrainer (MD2 & MD3) (July 5, 2023)
  • K222018 — Breathe+ (June 2, 2023)
  • K220565 — Hudson RCI Triflo II Incentive Deep Breathing Exerciser (October 25, 2022)
  • K203378 — Pulsehaler (March 31, 2021)
  • K192000 — D R Burton OxyPAP (February 19, 2020)
  • K181660 — Acapella Choice Blue Vibratory PEP Device (October 24, 2019)
  • K183108 — Combined Aerobika OPEP and VersaPAP device (August 16, 2019)
  • K182847 — Hudson RCI Voldyne Volumetric Exerciser (July 1, 2019)