FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

ROBOTRAC (TM) RETRACTOR ARM

K Number: K893121 · Decision Jun 1, 1989
Classifications
1
FEI Numbers
658
Registration Numbers
658
Same Product Code
99
Applicant Total
13
Review Days
37

Basic Information

Device Name
ROBOTRAC (TM) RETRACTOR ARM
K Number
K893121
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
AESCULAP INSTRUMENTS CORP.
Date Received
April 25, 1989
Decision Date
June 1, 1989
Product Code
GAD
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GAD Retractor

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