GECHO
K-Number: K250120 · 2025-07-14
ApplicantNarnar, LLC
Decision Date2025-07-14
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
GECHO is the device name listed in this FDA 510(k) record. The listed applicant is Narnar, LLC. It received FDA 510(k) clearance on 2025-07-14 under 510(k) number K250120. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the GECHO?
GECHO is a medical device that received FDA 510(k) clearance on 2025-07-14. The listed applicant is Narnar, LLC. The 510(k) number is K250120.
When did GECHO receive FDA 510(k) clearance?
GECHO received FDA 510(k) clearance on 2025-07-14, under 510(k) number K250120.
Who is the listed applicant for GECHO?
The FDA 510(k) record lists Narnar, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GECHO?
The FDA product code for GECHO is LLZ.
Related Devices (Code: LLZ)
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
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