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

NANO TECH AND SUPER NANO ACUPUNCTURE NEEDLES

K Number: K031060 · Decision Jul 11, 2003
Classifications
1
FEI Numbers
70
Registration Numbers
70
Same Product Code
90
Applicant Total
11
Review Days
99

Basic Information

Device Name
NANO TECH AND SUPER NANO ACUPUNCTURE NEEDLES
K Number
K031060
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5580
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
LHASA MEDICAL, INC.
Date Received
April 3, 2003
Decision Date
July 11, 2003
Product Code
MQX
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
MQX Needle, Acupuncture, Single Use

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K963299 HWA-TO ACUPUNCTURE NEEDLES
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K962916 HUA-XIA ACUPUNCTURE NEEDLES
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