Product Code: GWZ FDA class 1 21 CFR 882.1700

Percussor

Neurology

The Percussor is a neurological examination instrument used by clinicians to assess deep tendon reflexes by delivering a controlled percussive tap to tendons, aiding in the evaluation of the peripheral and central nervous systems. It is an FDA Class 1 device subject only to general controls, and it is GMP exempt, reflecting its low risk and simple function. The product code is GWZ, regulated under 21 CFR 882.1700 in the Neurology specialty. No other special flags apply to this device.

510(k)s
11
FEI Numbers
62
Registration Numbers
62
Unique Applicants
7
Years Active
10

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Basic Information

Product Code
GWZ
Device Class
FDA class 1
Regulation Number
882.1700
Medical Specialty
Neurology
Review Panel
NE
Submission Type
4

Device Characteristics

GMP Exempt
Implant
Life Sustain/Support
Third Party
Summary Malfunction Reporting

510(k) Clearance History

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Related 510(k) Clearances

This FDA classification is associated with 11 510(k) clearances via K numbers.

K Number Device Name
K891571 PERCUSSION HAMMER
K852716 TAYLOR PERCUSSION HAMMER SS 410 OR 420
K851748 1/310, 1-320 PERCUSSION HAMMERS,TAYLOR, DEJERINE
K840314 CAT 10-NEUROLOGY DEVICE
K834178 H.R. JAKOBI SURG. INSTR. #10 34/36
K834170 OP-CON SURG. INSTRUMENT #10
K810054 RICA (DIAGNOSTIC INSTRUMENTS)
K803148 CONPHAR PERCUSSION HAMMER(TAYLOR)
K803174 CONPHAR PERCUSSION HAMMER(BUCK TYPE)
K791337 TAYLOR NEUROLOGICAL HAMMER
K791336 BUCKS NEUROLOGICAL HAMMER

FEI Numbers

This FDA classification entry is associated with 62 FEI numbers. Click on an entry to view related FDA registrations.

Registration Numbers

This FDA classification entry is associated with 62 registration numbers. Click on an entry to view related FDA registrations.