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)

PATIENT LATEX EXAMINATION GLOVE (PREPOWDERED)

K-Number: K971629 · 1997-08-06

Decision Date1997-08-06
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PATIENT LATEX EXAMINATION GLOVE (PREPOWDERED) is the device name listed in this FDA 510(k) record. The listed applicant is Besglove Medicare Sdn. Bhd.. It received FDA 510(k) clearance on 1997-08-06 under 510(k) number K971629. 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 PATIENT LATEX EXAMINATION GLOVE (PREPOWDERED)?

PATIENT LATEX EXAMINATION GLOVE (PREPOWDERED) is a medical device that received FDA 510(k) clearance on 1997-08-06. The listed applicant is Besglove Medicare Sdn. Bhd.. The 510(k) number is K971629.

When did PATIENT LATEX EXAMINATION GLOVE (PREPOWDERED) receive FDA 510(k) clearance?

PATIENT LATEX EXAMINATION GLOVE (PREPOWDERED) received FDA 510(k) clearance on 1997-08-06, under 510(k) number K971629.

Who is the listed applicant for PATIENT LATEX EXAMINATION GLOVE (PREPOWDERED)?

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

What is the FDA product code for PATIENT LATEX EXAMINATION GLOVE (PREPOWDERED)?

The FDA product code for PATIENT LATEX EXAMINATION GLOVE (PREPOWDERED) 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 Besglove Medicare 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 22 devices →

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.

↑