LUER-LOCK EXTENSION SET
K-Number: K770174 · 1977-03-30
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Device Summary
Frequently Asked Questions
What is the LUER-LOCK EXTENSION SET?
LUER-LOCK EXTENSION SET is a medical device that received FDA 510(k) clearance on 1977-03-30. The listed applicant is American Viggo. The 510(k) number is K770174.
When did LUER-LOCK EXTENSION SET receive FDA 510(k) clearance?
LUER-LOCK EXTENSION SET received FDA 510(k) clearance on 1977-03-30, under 510(k) number K770174.
Who is the listed applicant for LUER-LOCK EXTENSION SET?
The FDA 510(k) record lists American Viggo as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LUER-LOCK EXTENSION SET?
The FDA product code for LUER-LOCK EXTENSION SET is FPK.
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 American Viggo 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: FPK)
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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