HEIFETZ INTRACRANIAL ANEURYSM CLIPS
K-Number: K832795 · 1983-11-25
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Device Summary
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.
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.
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