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FDA 510(k)

STERILE SURGICAL LATEX GLOVES

K-Number: K882715 · 1988-11-08

Decision Date1988-11-08
Product CodeKGO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STERILE SURGICAL LATEX GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Plastic Materials of Puerto Rico, Inc.. It received FDA 510(k) clearance on 1988-11-08 under 510(k) number K882715. The device is classified under product code KGO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERILE SURGICAL LATEX GLOVES?

STERILE SURGICAL LATEX GLOVES is a medical device that received FDA 510(k) clearance on 1988-11-08. The listed applicant is Plastic Materials of Puerto Rico, Inc.. The 510(k) number is K882715.

When did STERILE SURGICAL LATEX GLOVES receive FDA 510(k) clearance?

STERILE SURGICAL LATEX GLOVES received FDA 510(k) clearance on 1988-11-08, under 510(k) number K882715.

Who is the listed applicant for STERILE SURGICAL LATEX GLOVES?

The FDA 510(k) record lists Plastic Materials of Puerto Rico, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STERILE SURGICAL LATEX GLOVES?

The FDA product code for STERILE SURGICAL LATEX GLOVES is KGO.

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: KGO)

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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