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SOLOSTICK (AMPLATZ DILATOR NEEDLE)

Page Type
Cleared 510(K)
510(k) Number
K896096
510(k) Type
Traditional
Applicant
MICROVENA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/10/1990
Days to Decision
172 days

SOLOSTICK (AMPLATZ DILATOR NEEDLE)

Page Type
Cleared 510(K)
510(k) Number
K896096
510(k) Type
Traditional
Applicant
MICROVENA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/10/1990
Days to Decision
172 days