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SURELITE AND SURELITE XL BLOOD LANCET

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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