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GLUCOLET 2 AUTOMATIC LANCING DEVICE FOR OB. BLOOD

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K902430
510(k) Type
Traditional
Applicant
HERAEUS KULZER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/2/1990
Days to Decision
63 days

GLUCOLET 2 AUTOMATIC LANCING DEVICE FOR OB. BLOOD

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K902430
510(k) Type
Traditional
Applicant
HERAEUS KULZER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/2/1990
Days to Decision
63 days