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RAPIDONE-OXY TEST

Page Type
Cleared 510(K)
510(k) Number
K014101
510(k) Type
Traditional
Applicant
AMERICAN BIO MEDICA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/20/2002
Days to Decision
97 days
Submission Type
Summary

RAPIDONE-OXY TEST

Page Type
Cleared 510(K)
510(k) Number
K014101
510(k) Type
Traditional
Applicant
AMERICAN BIO MEDICA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/20/2002
Days to Decision
97 days
Submission Type
Summary