LUTH-ALL SUB-Q NEEDLE SET
K-Number: K042666 · 2004-12-21
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Device Summary
Frequently Asked Questions
What is the LUTH-ALL SUB-Q NEEDLE SET?
LUTH-ALL SUB-Q NEEDLE SET is a medical device that received FDA 510(k) clearance on 2004-12-21. The listed applicant is Luth-All Medical Products, LLC. The 510(k) number is K042666.
When did LUTH-ALL SUB-Q NEEDLE SET receive FDA 510(k) clearance?
LUTH-ALL SUB-Q NEEDLE SET received FDA 510(k) clearance on 2004-12-21, under 510(k) number K042666.
Who is the listed applicant for LUTH-ALL SUB-Q NEEDLE SET?
The FDA 510(k) record lists Luth-All Medical Products, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LUTH-ALL SUB-Q NEEDLE SET?
The FDA product code for LUTH-ALL SUB-Q NEEDLE SET is FPA.
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.
Related Devices (Code: FPA)
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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