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NEEDLE COUNTER-SURE COUNT/30 CT. MAGN.

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K801257
510(k) Type
Traditional
Applicant
KLEEN TEST PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/4/1980
Days to Decision
7 days

NEEDLE COUNTER-SURE COUNT/30 CT. MAGN.

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K801257
510(k) Type
Traditional
Applicant
KLEEN TEST PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/4/1980
Days to Decision
7 days