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

NITRONOX(R), FIRST RESPONSE NITRONOX(TM)

K Number: K883833 · Decision Feb 17, 1989
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
54
Applicant Total
14
Review Days
161

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Basic Information

Device Name
NITRONOX(R), FIRST RESPONSE NITRONOX(TM)
K Number
K883833
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5330
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Matrix Medica, Inc.
Date Received
September 9, 1988
Decision Date
February 17, 1989
Product Code
BZR
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
BZR Mixer, Breathing Gases, Anesthesia Inhalation

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Other Clearances by Matrix Medica, Inc.

K Number Device Name
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K915353 MATRX MEDICAL MAXIMIZER 1000 AND 2000 VACUUM PUMP
K912661 MATRX, PYRAMID TRIANGLE BANDAGE
K900551 MATRX DISPOSABLE NON-INVASIVE GELLED PACING ELEC.
K895533 LIFE DEFENSE PLUS(TM), DEFIBRILLATOR/MONITOR/PACER
K895525 MATRX BATTERY CHARGER/DEFIBRILLATOR TESTER
K893219 MATRX DENTAL UNIT
K884879 CENTURION(TM) MIXER
Search all 14 clearances from Matrix Medica, Inc. →