VAS APPROXIMATOR
K-Number: K780520 · 1978-05-16
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Device Summary
Frequently Asked Questions
What is the VAS APPROXIMATOR?
VAS APPROXIMATOR is a medical device that received FDA 510(k) clearance on 1978-05-16. The listed applicant is Edward Weck, Inc.. The 510(k) number is K780520.
When did VAS APPROXIMATOR receive FDA 510(k) clearance?
VAS APPROXIMATOR received FDA 510(k) clearance on 1978-05-16, under 510(k) number K780520.
Who is the listed applicant for VAS APPROXIMATOR?
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 VAS APPROXIMATOR?
The FDA product code for VAS APPROXIMATOR is HAO.
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: HAO)
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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