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)

LATEX EXAMINATION GLOVES(MFG: MODLOOK INDUSTRIES)

K-Number: K904641 · 1990-10-19

Decision Date1990-10-19
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LATEX EXAMINATION GLOVES(MFG: MODLOOK INDUSTRIES) is the device name listed in this FDA 510(k) record. The listed applicant is Predex Co. , Ltd.. It received FDA 510(k) clearance on 1990-10-19 under 510(k) number K904641. 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 LATEX EXAMINATION GLOVES(MFG: MODLOOK INDUSTRIES)?

LATEX EXAMINATION GLOVES(MFG: MODLOOK INDUSTRIES) is a medical device that received FDA 510(k) clearance on 1990-10-19. The listed applicant is Predex Co. , Ltd.. The 510(k) number is K904641.

When did LATEX EXAMINATION GLOVES(MFG: MODLOOK INDUSTRIES) receive FDA 510(k) clearance?

LATEX EXAMINATION GLOVES(MFG: MODLOOK INDUSTRIES) received FDA 510(k) clearance on 1990-10-19, under 510(k) number K904641.

Who is the listed applicant for LATEX EXAMINATION GLOVES(MFG: MODLOOK INDUSTRIES)?

The FDA 510(k) record lists Predex Co. , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LATEX EXAMINATION GLOVES(MFG: MODLOOK INDUSTRIES)?

The FDA product code for LATEX EXAMINATION GLOVES(MFG: MODLOOK INDUSTRIES) 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 Predex Co. , Ltd. 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.

↑