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FDA 510(k)

N PROTEIN STANDARD PY

K-Number: K962410 · 1996-07-16

ApplicantBehring Diagnostics, Inc.
Decision Date1996-07-16
Product CodeJIX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

N PROTEIN STANDARD PY 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 1996-07-16 under 510(k) number K962410. The device is classified under product code JIX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the N PROTEIN STANDARD PY?

N PROTEIN STANDARD PY is a medical device that received FDA 510(k) clearance on 1996-07-16. The listed applicant is Behring Diagnostics, Inc.. The 510(k) number is K962410.

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

N PROTEIN STANDARD PY received FDA 510(k) clearance on 1996-07-16, under 510(k) number K962410.

Who is the listed applicant for N PROTEIN STANDARD PY?

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 PY?

The FDA product code for N PROTEIN STANDARD PY is JIX.

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Related Devices (Code: JIX)

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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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