FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

MATRX MEDICAL MAXIMIZER 1000 AND 2000 VACUUM PUMP

K Number: K915353 · Decision Dec 27, 1991
Classifications
1
FEI Numbers
111
Registration Numbers
111
Same Product Code
283
Applicant Total
14
Review Days
31

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Basic Information

Device Name
MATRX MEDICAL MAXIMIZER 1000 AND 2000 VACUUM PUMP
K Number
K915353
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.6640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Matrix Medica, Inc.
Date Received
November 26, 1991
Decision Date
December 27, 1991
Product Code
EIA
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

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

Product Code Device Name
EIA Unit, Operative Dental

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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
K883833 NITRONOX(R), FIRST RESPONSE NITRONOX(TM)
K884879 CENTURION(TM) MIXER
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