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ULTRASYSTEM LINSCAN PROBE

Page Type
Cleared 510(K)
510(k) Number
K842811
510(k) Type
Traditional
Applicant
KELLEY DEVELOPMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/17/1984
Days to Decision
61 days

ULTRASYSTEM LINSCAN PROBE

Page Type
Cleared 510(K)
510(k) Number
K842811
510(k) Type
Traditional
Applicant
KELLEY DEVELOPMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/17/1984
Days to Decision
61 days