PLPT LDV(Low Dead Volume) LC(Luer-Cone) Sterile Syringe, PLPT LDV(Low Dead Volume) LL(Luer-Lock) Sterile Syringe
Summary
Poonglim Pharmatech, Inc. received 510(k) clearance for PLPT LDV(Low Dead Volume) LC(Luer-Cone) Sterile Syringe, PLPT LDV(Low Dead Volume) LL(Luer-Lock) Sterile Syringe, a QNQ device. Cleared on 2023-09-15.
Details
Source
510(k) Clearance
External ID
K221860
Action Date
2023-09-15
Status
Traditional
Category
device
Product Code
QNQ
Product Description
PLPT LDV(Low Dead Volume) LC(Luer-Cone) Sterile Syringe, PLPT LDV(Low Dead Volume) LL(Luer-Lock) Sterile Syringe. Product code: QNQ.
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. Poonglim Pharmatech, Inc. has received 2 total clearances in our database.
Poonglim Pharmatech, Inc. has 2 FDA actions in our database, including 2 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 Poonglim Pharmatech, Inc. have FDA actions?
Poonglim Pharmatech, Inc. has 2 FDA actions in our database, including 0 recalls and 2 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "K221860" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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