INNOVATIVE GLOVES, LATEX EXAMINATION GLOVES POWDERFREE
K-Number: K993222 · 1999-11-05
Advertisement
Device Summary
Frequently Asked Questions
What is the INNOVATIVE GLOVES, LATEX EXAMINATION GLOVES POWDERFREE?
INNOVATIVE GLOVES, LATEX EXAMINATION GLOVES POWDERFREE is a medical device that received FDA 510(k) clearance on 1999-11-05. The listed applicant is Innovative Gloves Co;, Ltd.. The 510(k) number is K993222.
When did INNOVATIVE GLOVES, LATEX EXAMINATION GLOVES POWDERFREE receive FDA 510(k) clearance?
INNOVATIVE GLOVES, LATEX EXAMINATION GLOVES POWDERFREE received FDA 510(k) clearance on 1999-11-05, under 510(k) number K993222.
Who is the listed applicant for INNOVATIVE GLOVES, LATEX EXAMINATION GLOVES POWDERFREE?
The FDA 510(k) record lists Innovative Gloves Co;, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INNOVATIVE GLOVES, LATEX EXAMINATION GLOVES POWDERFREE?
The FDA product code for INNOVATIVE GLOVES, LATEX EXAMINATION GLOVES POWDERFREE 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 Innovative Gloves 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.
Advertisement