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AESCULAP MANUAL ENDOSCOPIC INSTRUMENTS

Page Type
Cleared 510(K)
510(k) Number
K922576
510(k) Type
Traditional
Applicant
AESCULAP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/10/1993
Days to Decision
374 days
Submission Type
Statement

AESCULAP MANUAL ENDOSCOPIC INSTRUMENTS

Page Type
Cleared 510(K)
510(k) Number
K922576
510(k) Type
Traditional
Applicant
AESCULAP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/10/1993
Days to Decision
374 days
Submission Type
Statement