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510(k) K761118

Device
Hand Screw Clamp
Applicant
FRED SAMMONS, INC.
510(k) number
K761118
Product code
IOD
Decision
Substantially Equivalent (SESE)
Decision date
1976-12-02
Date received
1976-11-19
Regulation
890.5350
Classification name
Components, Exercise
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 IOD#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K831544DELUXE TRACTION EXERCISE GLOVE BK5035Fred Sammons, Inc.1983-06-24
K823648SURGICAL TUBINGFred Sammons, Inc.1983-01-21
K823822ANKLE WEIGHTSDanek Medical, Inc.1983-01-14
K823600SOLID WOOD CONEFred Sammons, Inc.1982-12-22
K813632COLOR CODED WEIGHT CUFFSFred Sammons, Inc.1982-01-19
K812319THERAPY BENCHKaye Products, Inc.1981-08-31
K790587CANVAS WEDGEMaddak, Inc.1979-04-03
K772414SANDBAGS, VARIOUS WEIGHTSFred Sammons, Inc.1978-02-01
K771030FLEXION MITTENSStat Medical Corp.1977-06-27
K761119SHEET METAL CLAMPFred Sammons, Inc.1976-12-02