Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MiroCam Capsule Endoscope System

K-Number: K180732 · 2018-11-08

Decision Date2018-11-08
Product CodeNEZ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MiroCam Capsule Endoscope System is the device name listed in this FDA 510(k) record. The listed applicant is Intromedic Co., Ltd.. It received FDA 510(k) clearance on 2018-11-08 under 510(k) number K180732. The device is classified under product code NEZ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MiroCam Capsule Endoscope System?

MiroCam Capsule Endoscope System is a medical device that received FDA 510(k) clearance on 2018-11-08. The listed applicant is Intromedic Co., Ltd.. The 510(k) number is K180732.

When did MiroCam Capsule Endoscope System receive FDA 510(k) clearance?

MiroCam Capsule Endoscope System received FDA 510(k) clearance on 2018-11-08, under 510(k) number K180732.

Who is the listed applicant for MiroCam Capsule Endoscope System?

The FDA 510(k) record lists Intromedic Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MiroCam Capsule Endoscope System?

The FDA product code for MiroCam Capsule Endoscope System is NEZ.

Other records listing Intromedic Co., Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: NEZ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.