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)

SYNTHETIC SURGICAL GLOVE-POWDERFREE NUZONE X2

K-Number: K041436 · 2004-08-20

Decision Date2004-08-20
Product CodeKGO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SYNTHETIC SURGICAL GLOVE-POWDERFREE NUZONE X2 is the device name listed in this FDA 510(k) record. The listed applicant is Terang Nusa Sdn Bhd. It received FDA 510(k) clearance on 2004-08-20 under 510(k) number K041436. 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 SYNTHETIC SURGICAL GLOVE-POWDERFREE NUZONE X2?

SYNTHETIC SURGICAL GLOVE-POWDERFREE NUZONE X2 is a medical device that received FDA 510(k) clearance on 2004-08-20. The listed applicant is Terang Nusa Sdn Bhd. The 510(k) number is K041436.

When did SYNTHETIC SURGICAL GLOVE-POWDERFREE NUZONE X2 receive FDA 510(k) clearance?

SYNTHETIC SURGICAL GLOVE-POWDERFREE NUZONE X2 received FDA 510(k) clearance on 2004-08-20, under 510(k) number K041436.

Who is the listed applicant for SYNTHETIC SURGICAL GLOVE-POWDERFREE NUZONE X2?

The FDA 510(k) record lists Terang Nusa Sdn Bhd as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SYNTHETIC SURGICAL GLOVE-POWDERFREE NUZONE X2?

The FDA product code for SYNTHETIC SURGICAL GLOVE-POWDERFREE NUZONE X2 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 Terang Nusa Sdn Bhd 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 24 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.

↑