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HOME BLOOD GLUCOSE MONITOR

Page Type
Cleared 510(K)
510(k) Number
K822486
510(k) Type
Traditional
Applicant
PHARMAQUEST CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/1982
Days to Decision
80 days

HOME BLOOD GLUCOSE MONITOR

Page Type
Cleared 510(K)
510(k) Number
K822486
510(k) Type
Traditional
Applicant
PHARMAQUEST CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/1982
Days to Decision
80 days