POWDERED VINYL PATIENT GLOVE
K-Number: K070046 · 2007-02-07
Advertisement
Device Summary
Frequently Asked Questions
What is the POWDERED VINYL PATIENT GLOVE?
POWDERED VINYL PATIENT GLOVE is a medical device that received FDA 510(k) clearance on 2007-02-07. The listed applicant is Shijiazhuang Lianhe Shunda Plastic Products Co., L. The 510(k) number is K070046.
When did POWDERED VINYL PATIENT GLOVE receive FDA 510(k) clearance?
POWDERED VINYL PATIENT GLOVE received FDA 510(k) clearance on 2007-02-07, under 510(k) number K070046.
Who is the listed applicant for POWDERED VINYL PATIENT GLOVE?
The FDA 510(k) record lists Shijiazhuang Lianhe Shunda Plastic Products Co., L as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POWDERED VINYL PATIENT GLOVE?
The FDA product code for POWDERED VINYL PATIENT GLOVE 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 Shijiazhuang Lianhe Shunda Plastic Products Co., L 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