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FDA 510(k)

NIL PATIENT EXAMINATION GLOVES (LATEX)

K-Number: K891834 · 1989-06-06

Decision Date1989-06-06
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NIL PATIENT EXAMINATION GLOVES (LATEX) is the device name listed in this FDA 510(k) record. The listed applicant is Glatex Sdn Bhd. It received FDA 510(k) clearance on 1989-06-06 under 510(k) number K891834. The device is classified under product code LYY. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NIL PATIENT EXAMINATION GLOVES (LATEX)?

NIL PATIENT EXAMINATION GLOVES (LATEX) is a medical device that received FDA 510(k) clearance on 1989-06-06. The listed applicant is Glatex Sdn Bhd. The 510(k) number is K891834.

When did NIL PATIENT EXAMINATION GLOVES (LATEX) receive FDA 510(k) clearance?

NIL PATIENT EXAMINATION GLOVES (LATEX) received FDA 510(k) clearance on 1989-06-06, under 510(k) number K891834.

Who is the listed applicant for NIL PATIENT EXAMINATION GLOVES (LATEX)?

The FDA 510(k) record lists Glatex Sdn Bhd as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NIL PATIENT EXAMINATION GLOVES (LATEX)?

The FDA product code for NIL PATIENT EXAMINATION GLOVES (LATEX) 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.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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