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)

STERILE LATEX SURGICAL GLOVE

K-Number: K892899 · 1990-01-17

Decision Date1990-01-17
Product CodeKGO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STERILE LATEX SURGICAL GLOVE is the device name listed in this FDA 510(k) record. The listed applicant is Tomarc (M) Sdn Bhd. It received FDA 510(k) clearance on 1990-01-17 under 510(k) number K892899. 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 STERILE LATEX SURGICAL GLOVE?

STERILE LATEX SURGICAL GLOVE is a medical device that received FDA 510(k) clearance on 1990-01-17. The listed applicant is Tomarc (M) Sdn Bhd. The 510(k) number is K892899.

When did STERILE LATEX SURGICAL GLOVE receive FDA 510(k) clearance?

STERILE LATEX SURGICAL GLOVE received FDA 510(k) clearance on 1990-01-17, under 510(k) number K892899.

Who is the listed applicant for STERILE LATEX SURGICAL GLOVE?

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

What is the FDA product code for STERILE LATEX SURGICAL GLOVE?

The FDA product code for STERILE LATEX SURGICAL GLOVE 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 Tomarc (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.

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.

↑