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CERULLO SUCTION REGULATOR

Page Type
Cleared 510(K)
510(k) Number
K880704
510(k) Type
Traditional
Applicant
AESCULAP INSTRUMENTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/29/1988
Days to Decision
36 days

CERULLO SUCTION REGULATOR

Page Type
Cleared 510(K)
510(k) Number
K880704
510(k) Type
Traditional
Applicant
AESCULAP INSTRUMENTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/29/1988
Days to Decision
36 days