ABRAMSON TRACHEA HOOK & RETRACTOR
K-Number: K771190 · 1977-07-11
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Device Summary
Frequently Asked Questions
What is the ABRAMSON TRACHEA HOOK & RETRACTOR?
ABRAMSON TRACHEA HOOK & RETRACTOR is a medical device that received FDA 510(k) clearance on 1977-07-11. The listed applicant is Edward Weck, Inc.. The 510(k) number is K771190.
When did ABRAMSON TRACHEA HOOK & RETRACTOR receive FDA 510(k) clearance?
ABRAMSON TRACHEA HOOK & RETRACTOR received FDA 510(k) clearance on 1977-07-11, under 510(k) number K771190.
Who is the listed applicant for ABRAMSON TRACHEA HOOK & RETRACTOR?
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 ABRAMSON TRACHEA HOOK & RETRACTOR?
The FDA product code for ABRAMSON TRACHEA HOOK & RETRACTOR is GDG.
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: GDG)
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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