510(k) K772406

Device
Aesthesiometer
Applicant
FRED SAMMONS, INC.
510(k) number
K772406
Product code
GXB
Decision
Substantially Equivalent (SESE)
Decision date
1978-01-06
Date received
1977-12-27
Regulation
882.1500
Classification name
Esthesiometer
Medical specialty
Neurology
Review panel
Neurology
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 GXB#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K143068Medical Monofilament Sensory Screening TooolMedical Monofilament Manufacturing2015-01-14
K933798NU-PREP GELCadwell Laboratories, Inc.1994-04-22
K871571NEUROTIPS(TM)Ulster Scientific, Inc.1987-06-18
K801907ALGESIOMETERRowan Products, Inc.1980-09-16
K771847TEMP-TESTERJablecki, Charles, Dr.1977-11-02
K761133AESTHESIOMETERFred Sammons, Inc.1976-12-02