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510(k) K780312

Device
AUTONOM
Applicant
AUTONOMIC EQUIPMENT SUPPLY CO,
510(k) number
K780312
Product code
KNM  
Decision
Substantially Equivalent (SESE)
Decision date
1978-04-05
Date received
1978-02-15
Regulation
890.5765
Classification name
Device, Pressure Applying
Medical specialty
Physical Medicine
Review panel
Physical Medicine
Device class
1
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Address
803 N. Front St. Suite 3 Mchenry IL US 60050 60050

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code KNM  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K811956AUTONORM & NERV-A-NORMAutonomic Equipment Supply Co,1981-07-31

Legacy Summary#

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FDA Review#

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