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FDA 510(k)

PLYMOUTH & LAWANA EXAM GLOVES

K-Number: K893149 · 1989-06-09

Decision Date1989-06-09
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PLYMOUTH & LAWANA EXAM GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Healthgard Medical Products Ltd. Partnership. It received FDA 510(k) clearance on 1989-06-09 under 510(k) number K893149. 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 PLYMOUTH & LAWANA EXAM GLOVES?

PLYMOUTH & LAWANA EXAM GLOVES is a medical device that received FDA 510(k) clearance on 1989-06-09. The listed applicant is Healthgard Medical Products Ltd. Partnership. The 510(k) number is K893149.

When did PLYMOUTH & LAWANA EXAM GLOVES receive FDA 510(k) clearance?

PLYMOUTH & LAWANA EXAM GLOVES received FDA 510(k) clearance on 1989-06-09, under 510(k) number K893149.

Who is the listed applicant for PLYMOUTH & LAWANA EXAM GLOVES?

The FDA 510(k) record lists Healthgard Medical Products Ltd. Partnership as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PLYMOUTH & LAWANA EXAM GLOVES?

The FDA product code for PLYMOUTH & LAWANA EXAM 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 Healthgard Medical Products Ltd. Partnership 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

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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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