FDA 510(k)

N PROTEIN STANDARD PLASMA (HUMAN)

K-Number: K880356 · 1988-04-07

Decision Date1988-04-07

Product CodeCFN

Advisory CommitteeIM

DecisionSubstantially Equivalent

Device Summary

N PROTEIN STANDARD PLASMA (HUMAN) 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 1988-04-07 under 510(k) number K880356. The device is classified under product code CFN. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the N PROTEIN STANDARD PLASMA (HUMAN)?

N PROTEIN STANDARD PLASMA (HUMAN) is a medical device that received FDA 510(k) clearance on 1988-04-07. The listed applicant is Behring Diagnostics, Inc.. The 510(k) number is K880356.

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

N PROTEIN STANDARD PLASMA (HUMAN) received FDA 510(k) clearance on 1988-04-07, under 510(k) number K880356.

Who is the listed applicant for N PROTEIN STANDARD PLASMA (HUMAN)?

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 PROTEIN STANDARD PLASMA (HUMAN)?

The FDA product code for N PROTEIN STANDARD PLASMA (HUMAN) is CFN.

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Other records listing Behring Diagnostics, Inc. as applicant

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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.