FDA 510(k)

THE PROTECTORS

K-Number: K801312 · 1980-06-17

Decision Date1980-06-17

Product Code

DecisionSubstantially Equivalent

Device Summary

THE PROTECTORS is the device name listed in this FDA 510(k) record. The listed applicant is Cooper Medical Devices Corp.. It received FDA 510(k) clearance on 1980-06-17 under 510(k) number K801312. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE PROTECTORS?

THE PROTECTORS is a medical device that received FDA 510(k) clearance on 1980-06-17. The listed applicant is Cooper Medical Devices Corp.. The 510(k) number is K801312.

When did THE PROTECTORS receive FDA 510(k) clearance?

THE PROTECTORS received FDA 510(k) clearance on 1980-06-17, under 510(k) number K801312.

Who is the listed applicant for THE PROTECTORS?

The FDA 510(k) record lists Cooper Medical Devices Corp. as the applicant. This does not by itself establish the device manufacturer.

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Other records listing Cooper Medical Devices Corp. as applicant

K802927SEBESTYEN IRRIGATING CONTACT LENS K802971LANDERS CONTACT LENS K801850CHARLES PNEUMATIC INTRAOCULAR SCISSORS K801411MAY ILLUMINATED/INFUSION PIC K800833VABRA ASPIRATOR K791898OCUTOME MODEL 8000

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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.