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)

PERRY POWDER-FREE GLOVES, STYLE 45G

K-Number: K923929 · 1993-02-10

Decision Date1993-02-10
Product CodeKGO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PERRY POWDER-FREE GLOVES, STYLE 45G is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew Perry. It received FDA 510(k) clearance on 1993-02-10 under 510(k) number K923929. The device is classified under product code KGO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERRY POWDER-FREE GLOVES, STYLE 45G?

PERRY POWDER-FREE GLOVES, STYLE 45G is a medical device that received FDA 510(k) clearance on 1993-02-10. The listed applicant is Smith & Nephew Perry. The 510(k) number is K923929.

When did PERRY POWDER-FREE GLOVES, STYLE 45G receive FDA 510(k) clearance?

PERRY POWDER-FREE GLOVES, STYLE 45G received FDA 510(k) clearance on 1993-02-10, under 510(k) number K923929.

Who is the listed applicant for PERRY POWDER-FREE GLOVES, STYLE 45G?

The FDA 510(k) record lists Smith & Nephew Perry as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PERRY POWDER-FREE GLOVES, STYLE 45G?

The FDA product code for PERRY POWDER-FREE GLOVES, STYLE 45G is KGO.

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 Smith & Nephew Perry 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.

View all 10 devices →

Related Devices (Code: KGO)

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.

↑