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MOTOR DRIVEN EXTIRPATION INSTRUMENTS

Page Type
Cleared 510(K)
510(k) Number
K904859
510(k) Type
Traditional
Applicant
AESCULAP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/15/1991
Days to Decision
137 days

MOTOR DRIVEN EXTIRPATION INSTRUMENTS

Page Type
Cleared 510(K)
510(k) Number
K904859
510(k) Type
Traditional
Applicant
AESCULAP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/15/1991
Days to Decision
137 days