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)

SCIPOTEX POWDER FREE SURGICAL GLOVES (UNBEADED)

K-Number: K943255 · 1995-03-07

Decision Date1995-03-07
Product CodeKGO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SCIPOTEX POWDER FREE SURGICAL GLOVES (UNBEADED) is the device name listed in this FDA 510(k) record. The listed applicant is Wembley Rubber Products (M) Sdn Bhd. It received FDA 510(k) clearance on 1995-03-07 under 510(k) number K943255. 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 SCIPOTEX POWDER FREE SURGICAL GLOVES (UNBEADED)?

SCIPOTEX POWDER FREE SURGICAL GLOVES (UNBEADED) is a medical device that received FDA 510(k) clearance on 1995-03-07. The listed applicant is Wembley Rubber Products (M) Sdn Bhd. The 510(k) number is K943255.

When did SCIPOTEX POWDER FREE SURGICAL GLOVES (UNBEADED) receive FDA 510(k) clearance?

SCIPOTEX POWDER FREE SURGICAL GLOVES (UNBEADED) received FDA 510(k) clearance on 1995-03-07, under 510(k) number K943255.

Who is the listed applicant for SCIPOTEX POWDER FREE SURGICAL GLOVES (UNBEADED)?

The FDA 510(k) record lists Wembley Rubber Products (M) Sdn Bhd as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SCIPOTEX POWDER FREE SURGICAL GLOVES (UNBEADED)?

The FDA product code for SCIPOTEX POWDER FREE SURGICAL GLOVES (UNBEADED) 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 Wembley Rubber Products (M) 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 61 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.

↑