FDA 510(k) FDA class 2 Substantially Equivalent 🇰🇷 South Korea

MiroCam® Capsule Endoscope System

K Number: K252617 · Decision May 8, 2026
Classifications
1
FEI Numbers
16
Registration Numbers
16
Same Product Code
46
Applicant Total
11
Review Days
262

Basic Information

Device Name
MiroCam® Capsule Endoscope System
K Number
K252617
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
876.1300
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Intromedic Co., Ltd.
Date Received
August 19, 2025
Decision Date
May 8, 2026
Product Code
NEZ
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
NEZ System, Imaging, Gastrointestinal, Wireless, Capsule

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (NEZ), ordered by most recent decision date.

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Other Clearances by Intromedic Co., Ltd.

K Number Device Name
K180732 MiroCam Capsule Endoscope System
K170438 MiroCam Capsule Endoscope System
K143663 MiroCam Capsule Endoscope System
K134005 MIROCAM CAPSULE ENDOSCOPE SYSTEM
K140751 MIROCAM CAPSULE ENDOSCOPE SYSTEM
K131131 E.G. SCAN(TM) II ESOPHAGOSCOPE SYSTEM
K123428 MIROCAM CAPSULE ENDOSCOPE SYSTEM
K120702 E.G. SCAN II ESPHAGOSCOPE SYSTEM
K111450 MIROCAM CAPSULE ENDOSCOPE SYSTEM
K111030 E.G. SCAN (TM) ESOPHAGOSCOPE SYSTEM
Search all 11 clearances from Intromedic Co., Ltd. →