MODIFICATION OF N PROTEIN STANDARD SL
K-Number: K991181 · 1999-06-01
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Device Summary
Frequently Asked Questions
What is the MODIFICATION OF N PROTEIN STANDARD SL?
MODIFICATION OF N PROTEIN STANDARD SL is a medical device that received FDA 510(k) clearance on 1999-06-01. The listed applicant is Dade Behring, Inc.. The 510(k) number is K991181.
When did MODIFICATION OF N PROTEIN STANDARD SL receive FDA 510(k) clearance?
MODIFICATION OF N PROTEIN STANDARD SL received FDA 510(k) clearance on 1999-06-01, under 510(k) number K991181.
Who is the listed applicant for MODIFICATION OF N PROTEIN STANDARD SL?
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 MODIFICATION OF N PROTEIN STANDARD SL?
The FDA product code for MODIFICATION OF N PROTEIN STANDARD SL is JIX.
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 Dade Behring, 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.
Related Devices (Code: JIX)
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
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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