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

VIRAGARD/VIRASHIELD

K Number: K820459 · Decision Jun 16, 1982
Classifications
1
FEI Numbers
87
Registration Numbers
87
Same Product Code
147
Applicant Total
29
Review Days
117

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Basic Information

Device Name
VIRAGARD/VIRASHIELD
K Number
K820459
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2850
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Tri-Med, Inc.
Date Received
February 19, 1982
Decision Date
June 16, 1982
Product Code
DRS
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
DRS Transducer, Blood-Pressure, Extravascular

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Other Clearances by Tri-Med, Inc.

K Number Device Name
K040112 TRIMED BEARING PLATE; TRIMED VOLAR BEARING PLATE
K030877 TRIMED RADIAL BULLET
K010545 TBW
K961863 PARACENTESIS TRAYS
K875224 HUDSON CRANINAL BURRS
K850747 TRI-MED MODEL 105 SPECIAL AIRWAY ADAPTOR
K850746 TRI-MED MODEL 126 SAMPLE LINE W/EXTENDED LIFE NAFI
K850745 TRI-MED MODEL 112 MOISTURE TRAP
K843681 RESPIRATION & HEART RATE MONITOR 530
K843285 TRI-MED 610 CAPNOSTAT GAS ANALYZER
Search all 29 clearances from Tri-Med, Inc. →