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SURELITE AND SURELITE XL BLOOD LANCET

Page Type
Cleared 510(K)
510(k) Number
K902416
510(k) Type
Traditional
Applicant
GAINOR MEDICAL EUROPE, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/1/1990
Days to Decision
62 days

SURELITE AND SURELITE XL BLOOD LANCET

Page Type
Cleared 510(K)
510(k) Number
K902416
510(k) Type
Traditional
Applicant
GAINOR MEDICAL EUROPE, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/1/1990
Days to Decision
62 days