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FDA 510(k)

SIS BLU (SISBLU-30-01);SIS BLU (SISBLU-15-01)

K-Number: K260997 · 2026-09-09

ApplicantEndoclot Plus Co., Ltd.
Decision Date2026-09-09
Product CodePLL
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SIS BLU (SISBLU-30-01);SIS BLU (SISBLU-15-01) is the device name listed in this FDA 510(k) record. The listed applicant is Endoclot Plus Co., Ltd.. It received FDA 510(k) clearance on 2026-09-09 under 510(k) number K260997. The device is classified under product code PLL. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIS BLU (SISBLU-30-01);SIS BLU (SISBLU-15-01)?

SIS BLU (SISBLU-30-01);SIS BLU (SISBLU-15-01) is a medical device that received FDA 510(k) clearance on 2026-09-09. The listed applicant is Endoclot Plus Co., Ltd.. The 510(k) number is K260997.

When did SIS BLU (SISBLU-30-01);SIS BLU (SISBLU-15-01) receive FDA 510(k) clearance?

SIS BLU (SISBLU-30-01);SIS BLU (SISBLU-15-01) received FDA 510(k) clearance on 2026-09-09, under 510(k) number K260997.

Who is the listed applicant for SIS BLU (SISBLU-30-01);SIS BLU (SISBLU-15-01)?

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

What is the FDA product code for SIS BLU (SISBLU-30-01);SIS BLU (SISBLU-15-01)?

The FDA product code for SIS BLU (SISBLU-30-01);SIS BLU (SISBLU-15-01) is PLL.

Other records listing Endoclot Plus 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.

K190677EndoClotK191254EndoClotK162197EndoClot

Related Devices (Code: PLL)

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.

K241591Blue EyeThe Standard Co., Ltd.K220434Blue Eye (TS-905)The Standard Co., Ltd.K221385LiftUp (Ref. Nr.: 200.56.01), LiftUp Kit (Ref. Nr.: 200.56.02)Ovesco Endoscopy AGK200071Blue Beacon Submucosal Injectable SolutionMicro-Tech (Nanjing) Co., Ltd.K202376EverLift Submucosal Lifting AgentGi Supply, Inc.K191923EverLift Submucosal Lifting AgentGi Supply

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.

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