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FDA 510(k)

N LATEX RF KIT

K-Number: K071247 · 2007-08-08

ApplicantDade Behring, Inc.
Decision Date2007-08-08
Product CodeDHR
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

N LATEX RF KIT is the device name listed in this FDA 510(k) record. The listed applicant is Dade Behring, Inc.. It received FDA 510(k) clearance on 2007-08-08 under 510(k) number K071247. The device is classified under product code DHR. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the N LATEX RF KIT?

N LATEX RF KIT is a medical device that received FDA 510(k) clearance on 2007-08-08. The listed applicant is Dade Behring, Inc.. The 510(k) number is K071247.

When did N LATEX RF KIT receive FDA 510(k) clearance?

N LATEX RF KIT received FDA 510(k) clearance on 2007-08-08, under 510(k) number K071247.

Who is the listed applicant for N LATEX RF KIT?

The FDA 510(k) record lists Dade Behring, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for N LATEX RF KIT?

The FDA product code for N LATEX RF KIT is DHR.

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Related Devices (Code: DHR)

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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