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)

Safety Sliding Blood Collection Set

K-Number: K232781 · 2024-03-07

Decision Date2024-03-07
Product CodeJKA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

Safety Sliding Blood Collection Set is the device name listed in this FDA 510(k) record. The listed applicant is Jiangsu Caina Medical Co.,Ltd. It received FDA 510(k) clearance on 2024-03-07 under 510(k) number K232781. The device is classified under product code JKA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Safety Sliding Blood Collection Set?

Safety Sliding Blood Collection Set is a medical device that received FDA 510(k) clearance on 2024-03-07. The listed applicant is Jiangsu Caina Medical Co.,Ltd. The 510(k) number is K232781.

When did Safety Sliding Blood Collection Set receive FDA 510(k) clearance?

Safety Sliding Blood Collection Set received FDA 510(k) clearance on 2024-03-07, under 510(k) number K232781.

Who is the listed applicant for Safety Sliding Blood Collection Set?

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

What is the FDA product code for Safety Sliding Blood Collection Set?

The FDA product code for Safety Sliding Blood Collection Set is JKA.

Other records listing Jiangsu Caina Medical 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 15 devices →

Related Devices (Code: JKA)

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.