FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

BUCKS NEUROLOGICAL HAMMER

K Number: K791336 · Decision Aug 3, 1979
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
10
Applicant Total
6
Review Days
14

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Basic Information

Device Name
BUCKS NEUROLOGICAL HAMMER
K Number
K791336
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
882.1700
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Amdia Medical Products
Date Received
July 20, 1979
Decision Date
August 3, 1979
Product Code
GWZ
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GWZ Percussor

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GWZ), ordered by most recent decision date.

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Other Clearances by Amdia Medical Products

K Number Device Name
K791333 BOWLES STETHOSCOPE
K791335 NURSESCOPE
K791338 DUAL HEAD STETHOSCOPE
K791334 MULTISCOPE
K791337 TAYLOR NEUROLOGICAL HAMMER