FDA 510(k)

SNIPER, MODEL OR-3872XX SERIES

K-Number: K001251 · 2000-07-07

Decision Date2000-07-07

Product CodeDQX

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

SNIPER, MODEL OR-3872XX SERIES is the device name listed in this FDA 510(k) record. The listed applicant is Nipro Medical Corp.. It received FDA 510(k) clearance on 2000-07-07 under 510(k) number K001251. 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, MODEL OR-3872XX SERIES?

SNIPER, MODEL OR-3872XX SERIES is a medical device that received FDA 510(k) clearance on 2000-07-07. The listed applicant is Nipro Medical Corp.. The 510(k) number is K001251.

When did SNIPER, MODEL OR-3872XX SERIES receive FDA 510(k) clearance?

SNIPER, MODEL OR-3872XX SERIES received FDA 510(k) clearance on 2000-07-07, under 510(k) number K001251.

Who is the listed applicant for SNIPER, MODEL OR-3872XX SERIES?

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

What is the FDA product code for SNIPER, MODEL OR-3872XX SERIES?

The FDA product code for SNIPER, MODEL OR-3872XX SERIES is DQX.

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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.