510(k) K895395

Device
V. MUELLER RHOTON SELF-RETAINING BRAIN RETRACTOR
Applicant
Baxter Healthcare Corp
510(k) number
K895395
Product code
GZT
Decision
Substantially Equivalent (SESE)
Decision date
1989-10-19
Date received
1989-09-01
Regulation
882.4800
Classification name
Retractor, Self-Retaining, For Neurosurgery
Medical specialty
Neurology
Review panel
Neurology
Device class
2
Clearance type
Traditional
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
MATHEW NOWLAND
Address
7280 N. Caldwell Niles IL US 60648 60648

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF not indicated by FDA · openFDA JSON

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K071771INSTRUMED RETRACTORSInstrumed International, Inc.2007-08-02