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FDA 510(k)

N/T PROTEIN CONTROL SY/L, M AND H

K-Number: K955858 · 1996-02-21

Decision Date1996-02-21
Product CodeJJY
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

N/T PROTEIN CONTROL SY/L, M AND H 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 1996-02-21 under 510(k) number K955858. The device is classified under product code JJY. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the N/T PROTEIN CONTROL SY/L, M AND H?

N/T PROTEIN CONTROL SY/L, M AND H is a medical device that received FDA 510(k) clearance on 1996-02-21. The listed applicant is Behring Diagnostics, Inc.. The 510(k) number is K955858.

When did N/T PROTEIN CONTROL SY/L, M AND H receive FDA 510(k) clearance?

N/T PROTEIN CONTROL SY/L, M AND H received FDA 510(k) clearance on 1996-02-21, under 510(k) number K955858.

Who is the listed applicant for N/T PROTEIN CONTROL SY/L, M AND H?

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/T PROTEIN CONTROL SY/L, M AND H?

The FDA product code for N/T PROTEIN CONTROL SY/L, M AND H is JJY.

Related Clinical Trials

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.

Other records listing Behring Diagnostics, Inc. as applicant

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.

View all 145 devices →

Related Devices (Code: JJY)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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