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FDA 510(k)

OMED WOUND CLOSURE STRIPS

K-Number: K874813 · 1988-01-29

Decision Date1988-01-29
Product CodeFPX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

OMED WOUND CLOSURE STRIPS is the device name listed in this FDA 510(k) record. The listed applicant is Oxboro Medical Intl., Inc.. It received FDA 510(k) clearance on 1988-01-29 under 510(k) number K874813. The device is classified under product code FPX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OMED WOUND CLOSURE STRIPS?

OMED WOUND CLOSURE STRIPS is a medical device that received FDA 510(k) clearance on 1988-01-29. The listed applicant is Oxboro Medical Intl., Inc.. The 510(k) number is K874813.

When did OMED WOUND CLOSURE STRIPS receive FDA 510(k) clearance?

OMED WOUND CLOSURE STRIPS received FDA 510(k) clearance on 1988-01-29, under 510(k) number K874813.

Who is the listed applicant for OMED WOUND CLOSURE STRIPS?

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

What is the FDA product code for OMED WOUND CLOSURE STRIPS?

The FDA product code for OMED WOUND CLOSURE STRIPS is FPX.

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 Oxboro Medical Intl., 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: FPX)

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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