Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

QUIDEL MOLECULAR HMPV ASSAY

K-Number: K112490 · 2011-12-15

ApplicantQuidel Corp.
Decision Date2011-12-15
Product CodeOEM
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

QUIDEL MOLECULAR HMPV ASSAY is the device name listed in this FDA 510(k) record. The listed applicant is Quidel Corp.. It received FDA 510(k) clearance on 2011-12-15 under 510(k) number K112490. The device is classified under product code OEM. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUIDEL MOLECULAR HMPV ASSAY?

QUIDEL MOLECULAR HMPV ASSAY is a medical device that received FDA 510(k) clearance on 2011-12-15. The listed applicant is Quidel Corp.. The 510(k) number is K112490.

When did QUIDEL MOLECULAR HMPV ASSAY receive FDA 510(k) clearance?

QUIDEL MOLECULAR HMPV ASSAY received FDA 510(k) clearance on 2011-12-15, under 510(k) number K112490.

Who is the listed applicant for QUIDEL MOLECULAR HMPV ASSAY?

The FDA 510(k) record lists Quidel Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for QUIDEL MOLECULAR HMPV ASSAY?

The FDA product code for QUIDEL MOLECULAR HMPV ASSAY is OEM.

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 Quidel Corp. 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 93 devices →

Related Devices (Code: OEM)

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.

↑