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)

Huahong Sharps Container (HHR-I, HHR-II)

K-Number: K260845 · 2026-08-05

Decision Date2026-08-05
Product CodeMMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Huahong Sharps Container (HHR-I, HHR-II) is the device name listed in this FDA 510(k) record. The listed applicant is Tianjin Huahong Technology Co., Ltd.. It received FDA 510(k) clearance on 2026-08-05 under 510(k) number K260845. The device is classified under product code MMK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Huahong Sharps Container (HHR-I, HHR-II)?

Huahong Sharps Container (HHR-I, HHR-II) is a medical device that received FDA 510(k) clearance on 2026-08-05. The listed applicant is Tianjin Huahong Technology Co., Ltd.. The 510(k) number is K260845.

When did Huahong Sharps Container (HHR-I, HHR-II) receive FDA 510(k) clearance?

Huahong Sharps Container (HHR-I, HHR-II) received FDA 510(k) clearance on 2026-08-05, under 510(k) number K260845.

Who is the listed applicant for Huahong Sharps Container (HHR-I, HHR-II)?

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

What is the FDA product code for Huahong Sharps Container (HHR-I, HHR-II)?

The FDA product code for Huahong Sharps Container (HHR-I, HHR-II) is MMK.

Other records listing Tianjin Huahong Technology 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.

View all 14 devices →

Related Devices (Code: MMK)

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.