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ACCUTEMP PROBE

Page Type
Cleared 510(K)
510(k) Number
K960080
510(k) Type
Traditional
Applicant
KENTEC MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/1/1996
Days to Decision
111 days
Submission Type
Statement

ACCUTEMP PROBE

Page Type
Cleared 510(K)
510(k) Number
K960080
510(k) Type
Traditional
Applicant
KENTEC MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/1/1996
Days to Decision
111 days
Submission Type
Statement