Last synced on 23 September 2022 at 11:05 pm

MODIFIED DISP. CHIBA-TYPE NEEDLE DESIGNATED ASPI.

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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