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FDA 510(k)

N PROTEIN STANDARD UY

K-Number: K991705 · 1999-07-15

ApplicantDade Behring, Inc.
Decision Date1999-07-15
Product CodeJIT
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

N PROTEIN STANDARD UY 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 1999-07-15 under 510(k) number K991705. The device is classified under product code JIT. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the N PROTEIN STANDARD UY?

N PROTEIN STANDARD UY is a medical device that received FDA 510(k) clearance on 1999-07-15. The listed applicant is Dade Behring, Inc.. The 510(k) number is K991705.

When did N PROTEIN STANDARD UY receive FDA 510(k) clearance?

N PROTEIN STANDARD UY received FDA 510(k) clearance on 1999-07-15, under 510(k) number K991705.

Who is the listed applicant for N PROTEIN STANDARD UY?

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 PROTEIN STANDARD UY?

The FDA product code for N PROTEIN STANDARD UY is JIT.

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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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