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FDA 510(k)

NEOBASE NON-DERIVATIZED MSMS KIT, MODEL 3040

K-Number: K083130 · 2009-07-09

ApplicantPerkinelmer, Inc.
Decision Date2009-07-09
Product CodeNQL
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

NEOBASE NON-DERIVATIZED MSMS KIT, MODEL 3040 is the device name listed in this FDA 510(k) record. The listed applicant is Perkinelmer, Inc.. It received FDA 510(k) clearance on 2009-07-09 under 510(k) number K083130. The device is classified under product code NQL. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEOBASE NON-DERIVATIZED MSMS KIT, MODEL 3040?

NEOBASE NON-DERIVATIZED MSMS KIT, MODEL 3040 is a medical device that received FDA 510(k) clearance on 2009-07-09. The listed applicant is Perkinelmer, Inc.. The 510(k) number is K083130.

When did NEOBASE NON-DERIVATIZED MSMS KIT, MODEL 3040 receive FDA 510(k) clearance?

NEOBASE NON-DERIVATIZED MSMS KIT, MODEL 3040 received FDA 510(k) clearance on 2009-07-09, under 510(k) number K083130.

Who is the listed applicant for NEOBASE NON-DERIVATIZED MSMS KIT, MODEL 3040?

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?

The FDA product code for NEOBASE NON-DERIVATIZED MSMS KIT, MODEL 3040 is NQL.

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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.

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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.

K193103NeoBase 2 Non-derivatized MSMS KitPerkinelmer, Inc.K173568NeoBase 2 Non-derivatized MSMS KitWallac Oy, Subsidiary of Perkinelmer, Inc.K093916NEOBASE NON-DERIVATIZED MSMS KIT MODEL 3040-001UPerkinelmer, Inc.

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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