RecallHawk

PLPT LDV(Low Dead Volume) LC(Luer-Cone) Sterile Syringe, PLPT LDV(Low Dead Volume) LL(Luer-Lock) Sterile Syringe

Poonglim Pharmatech, Inc.

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.

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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