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FDA 510(k)

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

K-Number: K241190 · 2024-05-29

Decision Date2024-05-29
Product CodeQNQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PLPT LDV(Low Dead Volume) LC(Luer-Cone) Sterile Syringe; PLPT LDV(Low Dead Volume) LL(Luer-Lock) Sterile Syringe is a medical device manufactured by Poonglim Pharmatech, Inc.. It received FDA 510(k) clearance on 2024-05-29 under approval number K241190. The device is classified under product code QNQ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PLPT LDV(Low Dead Volume) LC(Luer-Cone) Sterile Syringe; PLPT LDV(Low Dead Volume) LL(Luer-Lock) Sterile Syringe?

PLPT LDV(Low Dead Volume) LC(Luer-Cone) Sterile Syringe; PLPT LDV(Low Dead Volume) LL(Luer-Lock) Sterile Syringe is a medical device that received FDA 510(k) clearance on 2024-05-29. It is manufactured by Poonglim Pharmatech, Inc.. The 510(k) number is K241190.

When was PLPT LDV(Low Dead Volume) LC(Luer-Cone) Sterile Syringe; PLPT LDV(Low Dead Volume) LL(Luer-Lock) Sterile Syringe approved by the FDA?

PLPT LDV(Low Dead Volume) LC(Luer-Cone) Sterile Syringe; PLPT LDV(Low Dead Volume) LL(Luer-Lock) Sterile Syringe received FDA 510(k) clearance on 2024-05-29, under approval number K241190.

What company makes PLPT LDV(Low Dead Volume) LC(Luer-Cone) Sterile Syringe; PLPT LDV(Low Dead Volume) LL(Luer-Lock) Sterile Syringe?

PLPT LDV(Low Dead Volume) LC(Luer-Cone) Sterile Syringe; PLPT LDV(Low Dead Volume) LL(Luer-Lock) Sterile Syringe is manufactured by Poonglim Pharmatech, Inc..

What is the FDA product code for PLPT LDV(Low Dead Volume) LC(Luer-Cone) Sterile Syringe; PLPT LDV(Low Dead Volume) LL(Luer-Lock) Sterile Syringe?

The FDA product code for PLPT LDV(Low Dead Volume) LC(Luer-Cone) Sterile Syringe; PLPT LDV(Low Dead Volume) LL(Luer-Lock) Sterile Syringe is QNQ.

Other Devices by Poonglim Pharmatech, Inc.

Related Devices (Code: QNQ)

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.