FDA 510(k)

NIPRO LUER ADAPTOR

K-Number: K992729 · 2000-01-13

Decision Date2000-01-13

Product CodeFMI

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

NIPRO LUER ADAPTOR 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 2000-01-13 under 510(k) number K992729. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NIPRO LUER ADAPTOR?

NIPRO LUER ADAPTOR is a medical device that received FDA 510(k) clearance on 2000-01-13. The listed applicant is Nipro Medical Corp.. The 510(k) number is K992729.

When did NIPRO LUER ADAPTOR receive FDA 510(k) clearance?

NIPRO LUER ADAPTOR received FDA 510(k) clearance on 2000-01-13, under 510(k) number K992729.

Who is the listed applicant for NIPRO LUER ADAPTOR?

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 NIPRO LUER ADAPTOR?

The FDA product code for NIPRO LUER ADAPTOR is FMI.

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Other records listing Nipro Medical Corp. as applicant

K093985NIPRO SAFETOUCH LOCKTAIL SAFETY FISTULA NEEDLE K081210NIPRO SAFETOUCH HUBER INFUSTION SET K072024NIPRO BLOOD TUBING SET WITH TRANSDUCER PROTECTOR AND PRIMING SET, MODEL A201-A219, V801-V806, 5M9634, 5M9693 K063368NIPRO BIOHOLE NEEDLE K063721NIPRO SAFETOUCH II GAMMA K052474NIPRO HYPODERMIC NEEDLE

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Related Devices (Code: FMI)

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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.