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

PRIMADO SURGICAL DRILL

K Number: K080722 · Decision Sep 17, 2008
Classifications
1
FEI Numbers
131
Registration Numbers
131
Same Product Code
90
Applicant Total
40
Review Days
188

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Basic Information

Device Name
PRIMADO SURGICAL DRILL
K Number
K080722
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.4250
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Nakanishi, Inc.
Date Received
March 13, 2008
Decision Date
September 17, 2008
Product Code
ERL
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
EN
Third Party
N

Classifications

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

Product Code Device Name
ERL Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece

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