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FDA 510(k)

OH-HARRIS

K-Number: K801388 · 1980-07-28

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1980-07-28
Product CodeKIH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

OH-HARRIS is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Professionals, Inc.. It received FDA 510(k) clearance on 1980-07-28 under 510(k) number K801388. The device is classified under product code KIH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OH-HARRIS?

OH-HARRIS is a medical device that received FDA 510(k) clearance on 1980-07-28. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K801388.

When did OH-HARRIS receive FDA 510(k) clearance?

OH-HARRIS received FDA 510(k) clearance on 1980-07-28, under 510(k) number K801388.

Who is the listed applicant for OH-HARRIS?

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

What is the FDA product code for OH-HARRIS?

The FDA product code for OH-HARRIS is KIH.

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Related Devices (Code: KIH)

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.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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