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TEKNAR PROSCAN ACCESSORY PROBE

Page Type
Cleared 510(K)
510(k) Number
K880659
510(k) Type
Traditional
Applicant
TEKNAR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/14/1988
Days to Decision
57 days

TEKNAR PROSCAN ACCESSORY PROBE

Page Type
Cleared 510(K)
510(k) Number
K880659
510(k) Type
Traditional
Applicant
TEKNAR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/14/1988
Days to Decision
57 days