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FDA 510(k)

PiccGuard

K-Number: K191195 · 2020-01-03

ApplicantPiccguard, LLC
Decision Date2020-01-03
Product CodePZW
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PiccGuard is the device name listed in this FDA 510(k) record. The listed applicant is Piccguard, LLC. It received FDA 510(k) clearance on 2020-01-03 under 510(k) number K191195. The device is classified under product code PZW. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PiccGuard?

PiccGuard is a medical device that received FDA 510(k) clearance on 2020-01-03. The listed applicant is Piccguard, LLC. The 510(k) number is K191195.

When did PiccGuard receive FDA 510(k) clearance?

PiccGuard received FDA 510(k) clearance on 2020-01-03, under 510(k) number K191195.

Who is the listed applicant for PiccGuard?

The FDA 510(k) record lists Piccguard, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PiccGuard?

The FDA product code for PiccGuard is PZW.

Related Devices (Code: PZW)

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.

K2205073M Curos Tamper-Evident Device, 3M Curos Tamper-Evident Device, Large3M Company

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.

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