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)

Alians Fragment Specific

K-Number: K170843 · 2017-06-16

Decision Date2017-06-16
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Alians Fragment Specific is the device name listed in this FDA 510(k) record. The listed applicant is Newclip Technics. It received FDA 510(k) clearance on 2017-06-16 under 510(k) number K170843. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Alians Fragment Specific?

Alians Fragment Specific is a medical device that received FDA 510(k) clearance on 2017-06-16. The listed applicant is Newclip Technics. The 510(k) number is K170843.

When did Alians Fragment Specific receive FDA 510(k) clearance?

Alians Fragment Specific received FDA 510(k) clearance on 2017-06-16, under 510(k) number K170843.

Who is the listed applicant for Alians Fragment Specific?

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

What is the FDA product code for Alians Fragment Specific?

The FDA product code for Alians Fragment Specific is HRS.

Other records listing Newclip Technics 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 26 devices →

Related Devices (Code: HRS)

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.