GOLDFARB LIVER CLAMP
K-Number: K760898 · 1976-12-29
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Device Summary
Frequently Asked Questions
What is the GOLDFARB LIVER CLAMP?
GOLDFARB LIVER CLAMP is a medical device that received FDA 510(k) clearance on 1976-12-29. The listed applicant is Edward Weck, Inc.. The 510(k) number is K760898.
When did GOLDFARB LIVER CLAMP receive FDA 510(k) clearance?
GOLDFARB LIVER CLAMP received FDA 510(k) clearance on 1976-12-29, under 510(k) number K760898.
Who is the listed applicant for GOLDFARB LIVER CLAMP?
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 GOLDFARB LIVER CLAMP?
The FDA product code for GOLDFARB LIVER CLAMP is GDJ.
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: GDJ)
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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