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FDA 510(k)

HEIFETZ INTRACRANIAL ANEURYSM CLIPS

K-Number: K832795 · 1983-11-25

Decision Date1983-11-25
Product CodeHCH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

HEIFETZ INTRACRANIAL ANEURYSM CLIPS is the device name listed in this FDA 510(k) record. The listed applicant is Edward Weck, Inc.. It received FDA 510(k) clearance on 1983-11-25 under 510(k) number K832795. 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 HEIFETZ INTRACRANIAL ANEURYSM CLIPS?

HEIFETZ INTRACRANIAL ANEURYSM CLIPS is a medical device that received FDA 510(k) clearance on 1983-11-25. The listed applicant is Edward Weck, Inc.. The 510(k) number is K832795.

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

HEIFETZ INTRACRANIAL ANEURYSM CLIPS received FDA 510(k) clearance on 1983-11-25, under 510(k) number K832795.

Who is the listed applicant for HEIFETZ INTRACRANIAL ANEURYSM CLIPS?

The FDA 510(k) record lists Edward Weck, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HEIFETZ INTRACRANIAL ANEURYSM CLIPS?

The FDA product code for HEIFETZ INTRACRANIAL 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 Edward Weck, Inc. 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 140 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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