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FDA 510(k)

CHARLES PNEUMATIC INTRAOCULAR SCISSORS

K-Number: K801850 · 1980-09-16

ApplicantCooper Medical Devices Corp.
Decision Date1980-09-16
Product CodeHQE
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

CHARLES PNEUMATIC INTRAOCULAR SCISSORS 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 1980-09-16 under 510(k) number K801850. The device is classified under product code HQE. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHARLES PNEUMATIC INTRAOCULAR SCISSORS?

CHARLES PNEUMATIC INTRAOCULAR SCISSORS is a medical device that received FDA 510(k) clearance on 1980-09-16. The listed applicant is Cooper Medical Devices Corp.. The 510(k) number is K801850.

When did CHARLES PNEUMATIC INTRAOCULAR SCISSORS receive FDA 510(k) clearance?

CHARLES PNEUMATIC INTRAOCULAR SCISSORS received FDA 510(k) clearance on 1980-09-16, under 510(k) number K801850.

Who is the listed applicant for CHARLES PNEUMATIC INTRAOCULAR SCISSORS?

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

What is the FDA product code for CHARLES PNEUMATIC INTRAOCULAR SCISSORS?

The FDA product code for CHARLES PNEUMATIC INTRAOCULAR SCISSORS is HQE.

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Other records listing Cooper Medical Devices Corp. as applicant

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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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