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)

HPI TRI-RADS VINYL RADIATION PROTECTION GLOVES

K-Number: K905086 · 1990-12-03

ApplicantHpi, Inc.
Decision Date1990-12-03
Product CodeIWP
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

HPI TRI-RADS VINYL RADIATION PROTECTION GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Hpi, Inc.. It received FDA 510(k) clearance on 1990-12-03 under 510(k) number K905086. The device is classified under product code IWP. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HPI TRI-RADS VINYL RADIATION PROTECTION GLOVES?

HPI TRI-RADS VINYL RADIATION PROTECTION GLOVES is a medical device that received FDA 510(k) clearance on 1990-12-03. The listed applicant is Hpi, Inc.. The 510(k) number is K905086.

When did HPI TRI-RADS VINYL RADIATION PROTECTION GLOVES receive FDA 510(k) clearance?

HPI TRI-RADS VINYL RADIATION PROTECTION GLOVES received FDA 510(k) clearance on 1990-12-03, under 510(k) number K905086.

Who is the listed applicant for HPI TRI-RADS VINYL RADIATION PROTECTION GLOVES?

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

What is the FDA product code for HPI TRI-RADS VINYL RADIATION PROTECTION GLOVES?

The FDA product code for HPI TRI-RADS VINYL RADIATION PROTECTION GLOVES is IWP.

Related Clinical Trials

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.

Other records listing Hpi, Inc. 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.

Related Devices (Code: IWP)

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.

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.

↑