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FDA 510(k)

LALAN GLOVES (PVT) LTD GLOVE, PATIENT EXAMINATION, LATEX

K-Number: K031386 · 2003-10-06

ApplicantLalan Gloves (Pvt) , Ltd.
Decision Date2003-10-06
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LALAN GLOVES (PVT) LTD GLOVE, PATIENT EXAMINATION, LATEX is the device name listed in this FDA 510(k) record. The listed applicant is Lalan Gloves (Pvt) , Ltd.. It received FDA 510(k) clearance on 2003-10-06 under 510(k) number K031386. 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 LALAN GLOVES (PVT) LTD GLOVE, PATIENT EXAMINATION, LATEX?

LALAN GLOVES (PVT) LTD GLOVE, PATIENT EXAMINATION, LATEX is a medical device that received FDA 510(k) clearance on 2003-10-06. The listed applicant is Lalan Gloves (Pvt) , Ltd.. The 510(k) number is K031386.

When did LALAN GLOVES (PVT) LTD GLOVE, PATIENT EXAMINATION, LATEX receive FDA 510(k) clearance?

LALAN GLOVES (PVT) LTD GLOVE, PATIENT EXAMINATION, LATEX received FDA 510(k) clearance on 2003-10-06, under 510(k) number K031386.

Who is the listed applicant for LALAN GLOVES (PVT) LTD GLOVE, PATIENT EXAMINATION, LATEX?

The FDA 510(k) record lists Lalan Gloves (Pvt) , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LALAN GLOVES (PVT) LTD GLOVE, PATIENT EXAMINATION, LATEX?

The FDA product code for LALAN GLOVES (PVT) LTD GLOVE, PATIENT EXAMINATION, LATEX is LYY.

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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.

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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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