VITROS Immunodiagnostic Products NT-proBNP II Reagent Pack
Summary
Ortho Clinical Diagnostics received 510(k) clearance for VITROS Immunodiagnostic Products NT-proBNP II Reagent Pack, a NBC device. Cleared on 2021-10-04.
Details
Source
510(k) Clearance
External ID
K201312
Action Date
2021-10-04
Status
Traditional
Category
device
Product Code
NBC
Product Description
VITROS Immunodiagnostic Products NT-proBNP II Reagent Pack. Product code: NBC.
Company
Context & Analysis
A 510(k) clearance means the FDA determined this device is substantially equivalent to a legally marketed device. This is one of 403 device clearances issued this month. Ortho Clinical Diagnostics has received 9 total clearances in our database.
Ortho Clinical Diagnostics has 14 FDA actions in our database, including 5 recalls and 9 clearances.
Frequently Asked Questions
What does 510(k) clearance mean?
A 510(k) is an FDA premarket submission demonstrating that a device is substantially equivalent to a legally marketed device. It does NOT mean FDA approval — it means the device is cleared for marketing because it's similar enough to an existing cleared device. Most medical devices reach market via 510(k) rather than full PMA approval.
How often does Ortho Clinical Diagnostics have FDA actions?
Ortho Clinical Diagnostics has 14 FDA actions in our database, including 5 recalls and 9 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "K201312" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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