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SPETEMP EF

Page Type
Cleared 510(K)
510(k) Number
K964809
510(k) Type
Traditional
Applicant
ULTRADENT PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/2/1997
Days to Decision
34 days
Submission Type
Statement

SPETEMP EF

Page Type
Cleared 510(K)
510(k) Number
K964809
510(k) Type
Traditional
Applicant
ULTRADENT PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/2/1997
Days to Decision
34 days
Submission Type
Statement