FDA 510(k)

N LATEX RF

K-Number: K942328 · 1994-10-20

Decision Date1994-10-20

Product CodeDHR

Advisory CommitteeIM

DecisionSubstantially Equivalent

Device Summary

N LATEX RF is the device name listed in this FDA 510(k) record. The listed applicant is Behring Diagnostics, Inc.. It received FDA 510(k) clearance on 1994-10-20 under 510(k) number K942328. 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?

N LATEX RF is a medical device that received FDA 510(k) clearance on 1994-10-20. The listed applicant is Behring Diagnostics, Inc.. The 510(k) number is K942328.

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

N LATEX RF received FDA 510(k) clearance on 1994-10-20, under 510(k) number K942328.

Who is the listed applicant for N LATEX RF?

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

What is the FDA product code for N LATEX RF?

The FDA product code for N LATEX RF is DHR.

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Other records listing Behring Diagnostics, Inc. as applicant

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Related Devices (Code: DHR)

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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.