Sterile Hypodermic Needles for Single Use
Summary
Azur Medical Company, Inc. received 510(k) clearance for Sterile Hypodermic Needles for Single Use, a FMI device. Cleared on 2021-10-14.
Details
Source
510(k) Clearance
External ID
K211214
Action Date
2021-10-14
Status
Traditional
Category
device
Product Code
FMI
Product Description
Sterile Hypodermic Needles for Single Use. Product code: FMI.
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. Azur Medical Company, Inc. has received 4 total clearances in our database.
Azur Medical Company, Inc. has 4 FDA actions in our database, including 4 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 Azur Medical Company, Inc. have FDA actions?
Azur Medical Company, Inc. has 4 FDA actions in our database, including 0 recalls and 4 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "K211214" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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