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FDA 510(k)

SNIPER ELITE MODEL-OR-E3872XX SERIES

K-Number: K011905 · 2001-08-28

ApplicantMaxxim Medical
Decision Date2001-08-28
Product CodeDQX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SNIPER ELITE MODEL-OR-E3872XX SERIES is the device name listed in this FDA 510(k) record. The listed applicant is Maxxim Medical. It received FDA 510(k) clearance on 2001-08-28 under 510(k) number K011905. The device is classified under product code DQX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SNIPER ELITE MODEL-OR-E3872XX SERIES?

SNIPER ELITE MODEL-OR-E3872XX SERIES is a medical device that received FDA 510(k) clearance on 2001-08-28. The listed applicant is Maxxim Medical. The 510(k) number is K011905.

When did SNIPER ELITE MODEL-OR-E3872XX SERIES receive FDA 510(k) clearance?

SNIPER ELITE MODEL-OR-E3872XX SERIES received FDA 510(k) clearance on 2001-08-28, under 510(k) number K011905.

Who is the listed applicant for SNIPER ELITE MODEL-OR-E3872XX SERIES?

The FDA 510(k) record lists Maxxim Medical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SNIPER ELITE MODEL-OR-E3872XX SERIES?

The FDA product code for SNIPER ELITE MODEL-OR-E3872XX SERIES is DQX.

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Related Devices (Code: DQX)

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.

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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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