LATEX DECONTAMINATION/PROCEDURE GLOVES (NON-STER)
K-Number: K890440 · 1989-05-12
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Device Summary
Frequently Asked Questions
What is the LATEX DECONTAMINATION/PROCEDURE GLOVES (NON-STER)?
LATEX DECONTAMINATION/PROCEDURE GLOVES (NON-STER) is a medical device that received FDA 510(k) clearance on 1989-05-12. The listed applicant is Tomarc (M) Sdn Bhd. The 510(k) number is K890440.
When did LATEX DECONTAMINATION/PROCEDURE GLOVES (NON-STER) receive FDA 510(k) clearance?
LATEX DECONTAMINATION/PROCEDURE GLOVES (NON-STER) received FDA 510(k) clearance on 1989-05-12, under 510(k) number K890440.
Who is the listed applicant for LATEX DECONTAMINATION/PROCEDURE GLOVES (NON-STER)?
The FDA 510(k) record lists Tomarc (M) Sdn Bhd as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LATEX DECONTAMINATION/PROCEDURE GLOVES (NON-STER)?
The FDA product code for LATEX DECONTAMINATION/PROCEDURE GLOVES (NON-STER) 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 Tomarc (M) 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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