FDA.reportPublic FDA data

510(k) K823350

Device
Elastic Compression Anklet
Applicant
PODIATRY PRODUCTS CORP.
510(k) number
K823350
Product code
FQL
Decision
Substantially Equivalent (SESE)
Decision date
1982-12-03
Date received
1982-11-09
Regulation
880.5780
Classification name
Stocking, Medical Support (For General Medical Purposes)
Medical specialty
General Hospital
Review panel
General Hospital
Device class
1
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Address
4221 Richmond Rd., NW Walker MI US 49534 49534

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code FQL#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K944240SOFT SOCKSilipos, Inc.1994-12-27
K823789ELASTIC COMPRESSION ANKLETOrthopaedic Resources Corp.1983-01-07
K821259VITASANSelomas, Inc.1982-06-23
K821260VITOFITSelomas, Inc.1982-06-23
K820484VENES CUSTON RXJung Products, Inc.1982-03-18