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)

NIL, NITRILE EXAMINATION GLOVE - POWDER FREE

K-Number: K993348 · 1999-11-19

Decision Date1999-11-19
Product CodeLZA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NIL, NITRILE EXAMINATION GLOVE - POWDER FREE is the device name listed in this FDA 510(k) record. The listed applicant is Sri Anusham Rubber Industries Pvt., Ltd.. It received FDA 510(k) clearance on 1999-11-19 under 510(k) number K993348. The device is classified under product code LZA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NIL, NITRILE EXAMINATION GLOVE - POWDER FREE?

NIL, NITRILE EXAMINATION GLOVE - POWDER FREE is a medical device that received FDA 510(k) clearance on 1999-11-19. The listed applicant is Sri Anusham Rubber Industries Pvt., Ltd.. The 510(k) number is K993348.

When did NIL, NITRILE EXAMINATION GLOVE - POWDER FREE receive FDA 510(k) clearance?

NIL, NITRILE EXAMINATION GLOVE - POWDER FREE received FDA 510(k) clearance on 1999-11-19, under 510(k) number K993348.

Who is the listed applicant for NIL, NITRILE EXAMINATION GLOVE - POWDER FREE?

The FDA 510(k) record lists Sri Anusham Rubber Industries Pvt., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NIL, NITRILE EXAMINATION GLOVE - POWDER FREE?

The FDA product code for NIL, NITRILE EXAMINATION GLOVE - POWDER FREE is LZA.

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 Sri Anusham Rubber Industries Pvt., 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: LZA)

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.

↑