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FDA 510(k)

LUTH-ALL SUB-Q NEEDLE SET

K-Number: K042666 · 2004-12-21

Decision Date2004-12-21
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LUTH-ALL SUB-Q NEEDLE SET is the device name listed in this FDA 510(k) record. The listed applicant is Luth-All Medical Products, LLC. It received FDA 510(k) clearance on 2004-12-21 under 510(k) number K042666. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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