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FDA 510(k)

PROTECT DROPS/SAME AS K874070

K-Number: K874194 · 1987-12-16

Decision Date1987-12-16
Product CodeEJK
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PROTECT DROPS/SAME AS K874070 is the device name listed in this FDA 510(k) record. The listed applicant is John O. Butler. It received FDA 510(k) clearance on 1987-12-16 under 510(k) number K874194. The device is classified under product code EJK. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROTECT DROPS/SAME AS K874070?

PROTECT DROPS/SAME AS K874070 is a medical device that received FDA 510(k) clearance on 1987-12-16. The listed applicant is John O. Butler. The 510(k) number is K874194.

When did PROTECT DROPS/SAME AS K874070 receive FDA 510(k) clearance?

PROTECT DROPS/SAME AS K874070 received FDA 510(k) clearance on 1987-12-16, under 510(k) number K874194.

Who is the listed applicant for PROTECT DROPS/SAME AS K874070?

The FDA 510(k) record lists John O. Butler as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PROTECT DROPS/SAME AS K874070?

The FDA product code for PROTECT DROPS/SAME AS K874070 is EJK.

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 John O. Butler 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: EJK)

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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