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SPIVE NEEDLE SYSTEM, MODIFICATION

Page Type
Cleared 510(K)
510(k) Number
K904013
510(k) Type
Traditional
Applicant
PASCALL MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/1/1990
Days to Decision
33 days

SPIVE NEEDLE SYSTEM, MODIFICATION

Page Type
Cleared 510(K)
510(k) Number
K904013
510(k) Type
Traditional
Applicant
PASCALL MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/1/1990
Days to Decision
33 days