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

Compass Steerable Needle with Adapters SRA-1-01 and SRA-2-01

K Number: K252874 · Decision Oct 8, 2025
Classifications
1
FEI Numbers
64
Registration Numbers
64
Same Product Code
32
Applicant Total
3
Review Days
28

Basic Information

Device Name
Compass Steerable Needle with Adapters SRA-1-01 and SRA-2-01
K Number
K252874
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
874.4680
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Serpex Medical, Inc.
Date Received
September 10, 2025
Decision Date
October 8, 2025
Product Code
KTI
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
KTI Bronchoscope Accessory

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K Number Device Name
K221206 Compass Steerable Needle
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