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

ZENITH HYLO AND VERTI-LIFT CHIROPRACTIC TABLES

K Number: K902971 · Decision Jul 26, 1990
Classifications
1
FEI Numbers
51
Registration Numbers
51
Same Product Code
101
Applicant Total
4
Review Days
20

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Basic Information

Device Name
ZENITH HYLO AND VERTI-LIFT CHIROPRACTIC TABLES
K Number
K902971
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.3760
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Williams Manufacturing Co.
Date Received
July 6, 1990
Decision Date
July 26, 1990
Product Code
INQ
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
INQ Table, Powered

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