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FDA 510(k)

MDI TRIGGER GUARD

K-Number: K040439 · 2004-07-08

Decision Date2004-07-08
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MDI TRIGGER GUARD is the device name listed in this FDA 510(k) record. The listed applicant is North American Technical Services (Nats) Corp.. It received FDA 510(k) clearance on 2004-07-08 under 510(k) number K040439. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MDI TRIGGER GUARD?

MDI TRIGGER GUARD is a medical device that received FDA 510(k) clearance on 2004-07-08. The listed applicant is North American Technical Services (Nats) Corp.. The 510(k) number is K040439.

When did MDI TRIGGER GUARD receive FDA 510(k) clearance?

MDI TRIGGER GUARD received FDA 510(k) clearance on 2004-07-08, under 510(k) number K040439.

Who is the listed applicant for MDI TRIGGER GUARD?

The FDA 510(k) record lists North American Technical Services (Nats) Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MDI TRIGGER GUARD?

The FDA product code for MDI TRIGGER GUARD is CAF.

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: CAF)

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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