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510(k) K900472

Device
SKYTRON MODEL 860 AND 800 COMP. SURGITA NEURO EQUI
Applicant
SKYTRON, DIV. THE KMW GROUP, INC.
510(k) number
K900472
Product code
HBN  
Decision
Substantially Equivalent (SESE)
Decision date
1990-09-04
Date received
1990-01-31
Regulation
882.4125
Classification name
Chair, Neurosurgical
Medical specialty
Neurology
Review panel
Neurology
Device class
1
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Contact
LARRY J PURCEY
Address
5000 36th St., SE Grand Rapids MI US 49512 49512

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code HBN  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K822426MCINTYRE MICROSCOPE STANDSurgi-Quip Inc.U1982-09-02
K822428SURGI-QUIP MICROSCOPE STANDSurgi-Quip Inc.U1982-09-02
K822012BINOCULAR OPERATING MICROSCOPES &Kelleher Corp.1982-07-30

Legacy Summary#

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FDA Review#

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