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)

BG PATIENT EXAMINATION GLOVES, NON-STERILE

K-Number: K961675 · 1996-07-25

Decision Date1996-07-25
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BG PATIENT EXAMINATION GLOVES, NON-STERILE is the device name listed in this FDA 510(k) record. The listed applicant is Biografik (Malaysia) Sdn Bhd. It received FDA 510(k) clearance on 1996-07-25 under 510(k) number K961675. The device is classified under product code LYY. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BG PATIENT EXAMINATION GLOVES, NON-STERILE?

BG PATIENT EXAMINATION GLOVES, NON-STERILE is a medical device that received FDA 510(k) clearance on 1996-07-25. The listed applicant is Biografik (Malaysia) Sdn Bhd. The 510(k) number is K961675.

When did BG PATIENT EXAMINATION GLOVES, NON-STERILE receive FDA 510(k) clearance?

BG PATIENT EXAMINATION GLOVES, NON-STERILE received FDA 510(k) clearance on 1996-07-25, under 510(k) number K961675.

Who is the listed applicant for BG PATIENT EXAMINATION GLOVES, NON-STERILE?

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

What is the FDA product code for BG PATIENT EXAMINATION GLOVES, NON-STERILE?

The FDA product code for BG PATIENT EXAMINATION GLOVES, NON-STERILE is LYY.

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 Biografik (Malaysia) 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: LYY)

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.

↑