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FDA 510(k)

STERILE SURGICAL NATURAL LATEX GLOVES

K-Number: K875349 · 1988-02-16

Decision Date1988-02-16
Product CodeKGO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STERILE SURGICAL NATURAL LATEX GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Marand Products, Inc.. It received FDA 510(k) clearance on 1988-02-16 under 510(k) number K875349. 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 NATURAL LATEX GLOVES?

STERILE SURGICAL NATURAL LATEX GLOVES is a medical device that received FDA 510(k) clearance on 1988-02-16. The listed applicant is Marand Products, Inc.. The 510(k) number is K875349.

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

STERILE SURGICAL NATURAL LATEX GLOVES received FDA 510(k) clearance on 1988-02-16, under 510(k) number K875349.

Who is the listed applicant for STERILE SURGICAL NATURAL LATEX GLOVES?

The FDA 510(k) record lists Marand Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

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

The FDA product code for STERILE SURGICAL NATURAL 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.

Other records listing Marand Products, Inc. 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: 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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