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MODIFIED EXEL 2400 ELITE/U & EXEL 2400E/U

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K900170
510(k) Type
Traditional
Applicant
ELSCINT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/25/1990
Days to Decision
194 days

MODIFIED EXEL 2400 ELITE/U & EXEL 2400E/U

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K900170
510(k) Type
Traditional
Applicant
ELSCINT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/25/1990
Days to Decision
194 days