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FDA 510(k)

OCO PREPARATIONS

K-Number: K874396 · 1988-05-18

ApplicantWilliams Importing Company, Inc.
Decision Date1988-05-18
Product CodeEJF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

OCO PREPARATIONS is the device name listed in this FDA 510(k) record. The listed applicant is Williams Importing Company, Inc.. It received FDA 510(k) clearance on 1988-05-18 under 510(k) number K874396. The device is classified under product code EJF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OCO PREPARATIONS?

OCO PREPARATIONS is a medical device that received FDA 510(k) clearance on 1988-05-18. The listed applicant is Williams Importing Company, Inc.. The 510(k) number is K874396.

When did OCO PREPARATIONS receive FDA 510(k) clearance?

OCO PREPARATIONS received FDA 510(k) clearance on 1988-05-18, under 510(k) number K874396.

Who is the listed applicant for OCO PREPARATIONS?

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

What is the FDA product code for OCO PREPARATIONS?

The FDA product code for OCO PREPARATIONS is EJF.

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Related Devices (Code: EJF)

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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