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

HR UNIT

K Number: K782148 · Decision Jan 8, 1979
Classifications
1
FEI Numbers
2
Registration Numbers
2
Same Product Code
0
Applicant Total
47
Review Days
17

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Basic Information

Device Name
HR UNIT
K Number
K782148
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.3025
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Parke-Davis Co.
Date Received
December 22, 1978
Decision Date
January 8, 1979
Product Code
IQP
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

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

Product Code Device Name
IQP Rotator, Transverse

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K851327 DESERET ARTERIAL CATHETER
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