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FDA 510(k)

K2 MOBILE

K-Number: K200693 · 2020-11-19

ApplicantHulaser, Inc.
Decision Date2020-11-19
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

K2 MOBILE is the device name listed in this FDA 510(k) record. The listed applicant is Hulaser, Inc.. It received FDA 510(k) clearance on 2020-11-19 under 510(k) number K200693. The device is classified under product code GEX. It was reviewed by the SU advisory panel. Product code GEX falls under the category of Gastroenterology, which includes gastrointestinal diagnostic and therapeutic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the K2 MOBILE?

K2 MOBILE is a medical device that received FDA 510(k) clearance on 2020-11-19. The listed applicant is Hulaser, Inc.. The 510(k) number is K200693.

When did K2 MOBILE receive FDA 510(k) clearance?

K2 MOBILE received FDA 510(k) clearance on 2020-11-19, under 510(k) number K200693.

Who is the listed applicant for K2 MOBILE?

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

What is the FDA product code for K2 MOBILE?

The FDA product code for K2 MOBILE is GEX. This falls under the Gastroenterology category.

Related Devices (Code: GEX)

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.

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Official Source

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

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