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)

YASARGIL ANEURYSM CLIPS

K-Number: K772200 · 1977-12-08

Decision Date1977-12-08
Product CodeHCH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

YASARGIL ANEURYSM CLIPS is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap Instruments Corp.. It received FDA 510(k) clearance on 1977-12-08 under 510(k) number K772200. The device is classified under product code HCH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the YASARGIL ANEURYSM CLIPS?

YASARGIL ANEURYSM CLIPS is a medical device that received FDA 510(k) clearance on 1977-12-08. The listed applicant is Aesculap Instruments Corp.. The 510(k) number is K772200.

When did YASARGIL ANEURYSM CLIPS receive FDA 510(k) clearance?

YASARGIL ANEURYSM CLIPS received FDA 510(k) clearance on 1977-12-08, under 510(k) number K772200.

Who is the listed applicant for YASARGIL ANEURYSM CLIPS?

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

What is the FDA product code for YASARGIL ANEURYSM CLIPS?

The FDA product code for YASARGIL ANEURYSM CLIPS is HCH.

Related Clinical Trials

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.

Other records listing Aesculap Instruments Corp. 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 13 devices →

Related Devices (Code: HCH)

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.

↑