NON-STERILE LATEX DENTAL PROCEDURE GLOVES
K-Number: K903857 · 1990-10-29
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Device Summary
Frequently Asked Questions
What is the NON-STERILE LATEX DENTAL PROCEDURE GLOVES?
NON-STERILE LATEX DENTAL PROCEDURE GLOVES is a medical device that received FDA 510(k) clearance on 1990-10-29. The listed applicant is Formtex Medical Sdn. Bhd.. The 510(k) number is K903857.
When did NON-STERILE LATEX DENTAL PROCEDURE GLOVES receive FDA 510(k) clearance?
NON-STERILE LATEX DENTAL PROCEDURE GLOVES received FDA 510(k) clearance on 1990-10-29, under 510(k) number K903857.
Who is the listed applicant for NON-STERILE LATEX DENTAL PROCEDURE GLOVES?
The FDA 510(k) record lists Formtex Medical Sdn. Bhd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NON-STERILE LATEX DENTAL PROCEDURE GLOVES?
The FDA product code for NON-STERILE LATEX DENTAL PROCEDURE 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 Formtex Medical Sdn. Bhd. 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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