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

SQ.line KERRISON

K Number: K223596 · Decision Jun 29, 2023
Classifications
1
FEI Numbers
61
Registration Numbers
61
Same Product Code
35
Applicant Total
207
Review Days
209

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Basic Information

Device Name
SQ.line KERRISON
K Number
K223596
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4840
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Aesculap, Inc.
Date Received
December 2, 2022
Decision Date
June 29, 2023
Product Code
HAE
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
HAE Rongeur, Manual

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