FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

THERA-MIST TM VOLUMINA INCENT SPIROMETER, P40000

K Number: K903489 · Decision Dec 10, 1990
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
107
Applicant Total
12
Review Days
130

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Basic Information

Device Name
THERA-MIST TM VOLUMINA INCENT SPIROMETER, P40000
K Number
K903489
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5690
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Pegasus Research Corp.
Date Received
August 2, 1990
Decision Date
December 10, 1990
Product Code
BWF
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
BWF Spirometer, Therapeutic (Incentive)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (BWF), ordered by most recent decision date.

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Other Clearances by Pegasus Research Corp.

K Number Device Name
K122857 HOPE CONTINUOUS NEBULIZER MODEL HOPE-11310, HEART NEBULIZER MODEL HEART-100609, THERAMIST NEBULIZER MODEL THERAMIST-3100
K020700 PMH 5000 HEATED HUMIDIFIER FOR RESPIRATORY THERAPY
K013856 PMH 1000 HEATED HUMIDIFIER
K983783 HEATED HUMIDIFIER
K962534 THERA-MIST NEBULIZER MODEL-P3000
K946057 AQUALARM MOISTURE SENSOR MODEL P85000
K915890 AUTOCLAVABLE THERA-MIST HUMIDIFIER P3600, MODIFIED
K914465 AUTOCLAVABLE VERSION THERA-MIST NEBULIZER, P32000
K893942 THERA-MIST(TM) NEBULIZER, MODEL 30000
K894000 THERA-MIST HUMIDIFIER
Search all 12 clearances from Pegasus Research Corp. →