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

AESTHESIOMETER

K Number: K874300 · Decision Nov 6, 1987
Classifications
1
FEI Numbers
16
Registration Numbers
16
Same Product Code
1
Applicant Total
95
Review Days
17

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Basic Information

Device Name
AESTHESIOMETER
K Number
K874300
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
882.1200
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Orthopedic Systems, Inc.
Date Received
October 20, 1987
Decision Date
November 6, 1987
Product Code
GWI
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
GWI Discriminator, Two-Point

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Other Clearances by Orthopedic Systems, Inc.

K Number Device Name
K952495 ANCHORS AWAY SOFT TISSUE ATTACHMENT SYSTEM
K920256 SPINE MOTION ANALYZER WITH EMG
K910736 JACKSON MULTIPURPOSE OPERATING TABLE
K910031 PARK CITY SHOULDER POSITIONER
K903938 C FIT CUP
K892503 NUFFIELD TOTAL KNEE
K896678 SILICONE PLUG
K894283 COMPREHENSIVE SPINE MOTION ANALYZER
K890498 FREEMAN MODULAR HIP STEM RIDGED VERSION
K890331 FREEMAN TOTAL HIP SYSTEM RIDGED STEM
Search all 95 clearances from Orthopedic Systems, Inc. →