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KONICA LASER IMAGER LI-21

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K950359
510(k) Type
Traditional
Applicant
STORCH, AMINI, & MUNVES, P.C.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/6/1995
Days to Decision
222 days
Submission Type
Statement

KONICA LASER IMAGER LI-21

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K950359
510(k) Type
Traditional
Applicant
STORCH, AMINI, & MUNVES, P.C.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/6/1995
Days to Decision
222 days
Submission Type
Statement