NEOBASE NON-DERIVATIZED MSMS KIT MODEL 3040-001U
K-Number: K093916 · 2010-08-23
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Device Summary
Frequently Asked Questions
What is the NEOBASE NON-DERIVATIZED MSMS KIT MODEL 3040-001U?
NEOBASE NON-DERIVATIZED MSMS KIT MODEL 3040-001U is a medical device that received FDA 510(k) clearance on 2010-08-23. The listed applicant is Perkinelmer, Inc.. The 510(k) number is K093916.
When did NEOBASE NON-DERIVATIZED MSMS KIT MODEL 3040-001U receive FDA 510(k) clearance?
NEOBASE NON-DERIVATIZED MSMS KIT MODEL 3040-001U received FDA 510(k) clearance on 2010-08-23, under 510(k) number K093916.
Who is the listed applicant for NEOBASE NON-DERIVATIZED MSMS KIT MODEL 3040-001U?
The FDA 510(k) record lists Perkinelmer, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NEOBASE NON-DERIVATIZED MSMS KIT MODEL 3040-001U?
The FDA product code for NEOBASE NON-DERIVATIZED MSMS KIT MODEL 3040-001U is NQL.
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 Perkinelmer, 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: NQL)
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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