GWZ — Percussor Class I

FDA Device Classification

FDA product code GWZ covers "Percussor", a Class I medical device regulated under 21 CFR 882.1700. Submissions are reviewed by the Neurology panel. At least 11 recent 510(k) clearances have been granted under this product code.

Classification details

Product Code
GWZ
Device Class
Class I
Regulation Number
882.1700
Submission Type
510(k) Exempt
Review Panel
NE
Medical Specialty
Neurology
Implant
No

Recent 510(k) clearances

K-NumberApplicantDevice NameDate
K891571Sandal SurgicoPERCUSSION HAMMERMar 31, 1989
K852716Huxley InstrumentTAYLOR PERCUSSION HAMMER SS 410 OR 420Jul 26, 1985
K851748Artiberia1/310, 1-320 PERCUSSION HAMMERS,TAYLOR, DEJERINEJun 13, 1985
K840314Imm EnterprisesCAT 10-NEUROLOGY DEVICEFeb 23, 1984
K834170Imm EnterprisesOP-CON SURG. INSTRUMENT #10Feb 23, 1984
K834178Imm EnterprisesH.R. JAKOBI SURG. INSTR. #10 34/36Feb 23, 1984
K810054Robert I. Chien And AssocRICA (DIAGNOSTIC INSTRUMENTS)Jan 28, 1981
K803148ConpharCONPHAR PERCUSSION HAMMER(TAYLOR)Jan 8, 1981
K803174ConpharCONPHAR PERCUSSION HAMMER(BUCK TYPE)Dec 30, 1980
K791337Amdia Medical ProductsTAYLOR NEUROLOGICAL HAMMERAug 3, 1979
K791336Amdia Medical ProductsBUCKS NEUROLOGICAL HAMMERAug 3, 1979

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.