Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

VPC

K-Number: K190345 · 2019-05-16

ApplicantPAJUNK GmbH Medizintechnologie
Decision Date2019-05-16
Product CodeCAZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VPC is the device name listed in this FDA 510(k) record. The listed applicant is PAJUNK GmbH Medizintechnologie. It received FDA 510(k) clearance on 2019-05-16 under 510(k) number K190345. The device is classified under product code CAZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VPC?

VPC is a medical device that received FDA 510(k) clearance on 2019-05-16. The listed applicant is PAJUNK GmbH Medizintechnologie. The 510(k) number is K190345.

When did VPC receive FDA 510(k) clearance?

VPC received FDA 510(k) clearance on 2019-05-16, under 510(k) number K190345.

Who is the listed applicant for VPC?

The FDA 510(k) record lists PAJUNK GmbH Medizintechnologie as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VPC?

The FDA product code for VPC is CAZ.

Other records listing PAJUNK GmbH Medizintechnologie as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K243690SonoMSKK243682SonoPlex STIM; SonoPlex IIK250774SPROTTE® STANDARD (LUER/ NRFit®) Lumbar PunctureK243525SonoTAP and SonoTAP IIK241953SPROTTE® STANDARD (LUER/ NRFit®) AnesthesiologyK241954SonoBlock; SonoBlock II

View all 21 devices →

Related Devices (Code: CAZ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K222341Arrow 0.2 Micron Flat Filter, GVSArrow International, LLCK210983BD Epilor SyringeBecton, Dickinson and CompanyK201356Plastic LOR SyringeJiangsu Caina Medical Co.,LtdK202699E-Cath STIM acc. TsuiPAJUNK GmbH MedizintechnologieK161075Arrow Epidural Catheter KitTeleflexmedical, Inc.K153652ARROW FlexBlock Continuous Peripheral Nerve Block Catheter Kit/SetTeleflex, Inc.

Official Source

View on FDA Database →

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

↑