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FDA 510(k)

MARINA MEDICAL FINGER PROTECTORS

K-Number: K042534 · 2005-05-10

Decision Date2005-05-10
Product CodeKGO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MARINA MEDICAL FINGER PROTECTORS is the device name listed in this FDA 510(k) record. The listed applicant is Marina Medical Instruments, Inc.. It received FDA 510(k) clearance on 2005-05-10 under 510(k) number K042534. 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 MARINA MEDICAL FINGER PROTECTORS?

MARINA MEDICAL FINGER PROTECTORS is a medical device that received FDA 510(k) clearance on 2005-05-10. The listed applicant is Marina Medical Instruments, Inc.. The 510(k) number is K042534.

When did MARINA MEDICAL FINGER PROTECTORS receive FDA 510(k) clearance?

MARINA MEDICAL FINGER PROTECTORS received FDA 510(k) clearance on 2005-05-10, under 510(k) number K042534.

Who is the listed applicant for MARINA MEDICAL FINGER PROTECTORS?

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

What is the FDA product code for MARINA MEDICAL FINGER PROTECTORS?

The FDA product code for MARINA MEDICAL FINGER PROTECTORS 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 Marina Medical Instruments, 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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