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MSI STERNUM ASPIRATION NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K820070
510(k) Type
Traditional
Applicant
CREATIVE RESEARCH AND MFG., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/4/1982
Days to Decision
23 days

MSI STERNUM ASPIRATION NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K820070
510(k) Type
Traditional
Applicant
CREATIVE RESEARCH AND MFG., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/4/1982
Days to Decision
23 days