FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

ELT OR ERGONOMIC LIFT TRAINER

K Number: K890500 · Decision Jan 3, 1990
Classifications
1
FEI Numbers
101
Registration Numbers
101
Same Product Code
171
Applicant Total
2
Review Days
336

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Basic Information

Device Name
ELT OR ERGONOMIC LIFT TRAINER
K Number
K890500
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5050
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Physical Health Devices, Inc.
Date Received
February 1, 1989
Decision Date
January 3, 1990
Product Code
HCC
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
HCC Device, Biofeedback

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Other Clearances by Physical Health Devices, Inc.

K Number Device Name
K870568 BIO-PROMPT(TM)