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ROBOTRAC (TM) RETRACTOR ARM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K893121
510(k) Type
Traditional
Applicant
AESCULAP INSTRUMENTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/1/1989
Days to Decision
37 days

ROBOTRAC (TM) RETRACTOR ARM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K893121
510(k) Type
Traditional
Applicant
AESCULAP INSTRUMENTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/1/1989
Days to Decision
37 days