Product code GWZ— Neurology
1/310, 1-320 PERCUSSION HAMMERS,TAYLOR, DEJERINE
- Classification name
- Percussor
- Device class
- Class 1
- Regulation
- 21 CFR 882.1700
- Advisory panel
- Neurology
- Total cleared
- 11
- First cleared
- Most recent
Market context for product code GWZ
FDA has cleared devices under product code GWZ between 1979 and 1989, filed by 7 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.
Clearances per year
- 1989
- 1985
- 1984
- 1981
- 1980
- 1979
Top applicants under product code GWZ
Recent clearances under product code GWZ
- K891571 — PERCUSSION HAMMER
- K852716 — TAYLOR PERCUSSION HAMMER SS 410 OR 420
- K851748 — 1/310, 1-320 PERCUSSION HAMMERS,TAYLOR, DEJERINE
- K834170 — OP-CON SURG. INSTRUMENT #10
- K834178 — H.R. JAKOBI SURG. INSTR. #10 34/36
- K840314 — CAT 10-NEUROLOGY DEVICE
- K810054 — RICA (DIAGNOSTIC INSTRUMENTS)
- K803148 — CONPHAR PERCUSSION HAMMER(TAYLOR)
- K803174 — CONPHAR PERCUSSION HAMMER(BUCK TYPE)
- K791336 — BUCKS NEUROLOGICAL HAMMER
- K791337 — TAYLOR NEUROLOGICAL HAMMER
Data sourced from openFDA. This site is unofficial and independent of the FDA.