POLY-FLEX LATEX EXAMINATION GLOVES
K-Number: K895499 · 1989-11-16
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Device Summary
Frequently Asked Questions
What is the POLY-FLEX LATEX EXAMINATION GLOVES?
POLY-FLEX LATEX EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1989-11-16. The listed applicant is Pacific Delta Medical Supply. The 510(k) number is K895499.
When did POLY-FLEX LATEX EXAMINATION GLOVES receive FDA 510(k) clearance?
POLY-FLEX LATEX EXAMINATION GLOVES received FDA 510(k) clearance on 1989-11-16, under 510(k) number K895499.
Who is the listed applicant for POLY-FLEX LATEX EXAMINATION GLOVES?
The FDA 510(k) record lists Pacific Delta Medical Supply as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POLY-FLEX LATEX EXAMINATION GLOVES?
The FDA product code for POLY-FLEX LATEX EXAMINATION GLOVES 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 Pacific Delta Medical Supply 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.
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