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KQW — Goniometer, Nonpowered Class I

FDA Device Classification

Classification Details

Product Code
KQW
Device Class
Class I
Regulation Number
888.1520
Submission Type
Review Panel
NE
Medical Specialty
Orthopedic
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K926237sgarlato laboratoriesO'BRIEN GONIOMETERAugust 2, 1993
K901744biosearch medical productsDOBBHOFF(R) RETRIEVAL FORCEPSJuly 3, 1990
K870767twin city surgicalTHE (CROM) TESTERMarch 17, 1987
K850082chattanooga groupHAND HELD GONIOMETERApril 4, 1985
K831550fred sammonsFINGER BONIOMETER BK7506June 24, 1983
K812778telosTHE TELOS EQUIPMENTDecember 8, 1981
K810441fred sammonsUNIVERSAL GONIMETERFebruary 27, 1981
K801717fred sammonsBK-7511 BRASS GONIOMETERAugust 4, 1980
K801716fred sammonsBK-7505 RADIOPAQUE GONIOMETER, 8August 4, 1980
K801715fred sammonsBK-7497 BULB DYNAMOMETERAugust 4, 1980
K801718fred sammonsBK-7513 STAINLESS STEEL GONIOMETERAugust 4, 1980
K760301fred sammonsGONIOMETER, MED. INTER. STAND. BK-7512September 8, 1976
K760302fred sammonsGONIOMETER, INTER. STAND. LARGE, BK7514September 8, 1976