DISPOSABLE VINYL SYNTHETIC EXAM GLOVES, POWDERED
K-Number: K990081 · 1999-02-19
Advertisement
Device Summary
Frequently Asked Questions
What is the DISPOSABLE VINYL SYNTHETIC EXAM GLOVES, POWDERED?
DISPOSABLE VINYL SYNTHETIC EXAM GLOVES, POWDERED is a medical device that received FDA 510(k) clearance on 1999-02-19. The listed applicant is Shanghai Palomar Mountain Industries, Inc.. The 510(k) number is K990081.
When did DISPOSABLE VINYL SYNTHETIC EXAM GLOVES, POWDERED receive FDA 510(k) clearance?
DISPOSABLE VINYL SYNTHETIC EXAM GLOVES, POWDERED received FDA 510(k) clearance on 1999-02-19, under 510(k) number K990081.
Who is the listed applicant for DISPOSABLE VINYL SYNTHETIC EXAM GLOVES, POWDERED?
The FDA 510(k) record lists Shanghai Palomar Mountain Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DISPOSABLE VINYL SYNTHETIC EXAM GLOVES, POWDERED?
The FDA product code for DISPOSABLE VINYL SYNTHETIC EXAM GLOVES, POWDERED is LYZ.
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 Shanghai Palomar Mountain Industries, Inc. 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: LYZ)
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