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)

UNISEAL GLOVES LOW PROTEIN POWDERED

K-Number: K981979 · 1998-11-30

Decision Date1998-11-30
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

UNISEAL GLOVES LOW PROTEIN POWDERED is the device name listed in this FDA 510(k) record. The listed applicant is American Healthcare Products (M) Sdn Bhd. It received FDA 510(k) clearance on 1998-11-30 under 510(k) number K981979. 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 UNISEAL GLOVES LOW PROTEIN POWDERED?

UNISEAL GLOVES LOW PROTEIN POWDERED is a medical device that received FDA 510(k) clearance on 1998-11-30. The listed applicant is American Healthcare Products (M) Sdn Bhd. The 510(k) number is K981979.

When did UNISEAL GLOVES LOW PROTEIN POWDERED receive FDA 510(k) clearance?

UNISEAL GLOVES LOW PROTEIN POWDERED received FDA 510(k) clearance on 1998-11-30, under 510(k) number K981979.

Who is the listed applicant for UNISEAL GLOVES LOW PROTEIN POWDERED?

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

What is the FDA product code for UNISEAL GLOVES LOW PROTEIN POWDERED?

The FDA product code for UNISEAL GLOVES LOW PROTEIN POWDERED 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 American Healthcare 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.

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.

↑