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MODIFIED DISP. CHIBA-TYPE NEEDLE DESIGNATED ASPI.

Page Type
Cleared 510(K)
510(k) Number
K896019
510(k) Type
Traditional
Applicant
DLP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/3/1990
Days to Decision
79 days

MODIFIED DISP. CHIBA-TYPE NEEDLE DESIGNATED ASPI.

Page Type
Cleared 510(K)
510(k) Number
K896019
510(k) Type
Traditional
Applicant
DLP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/3/1990
Days to Decision
79 days