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FDA 510(k)

RESUBMITTED DIODE LASER COAGULATOR

K-Number: K882372 · 1988-08-02

ApplicantCooperVision, Inc.
Decision Date1988-08-02
Product CodeHQF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

RESUBMITTED DIODE LASER COAGULATOR is the device name listed in this FDA 510(k) record. The listed applicant is CooperVision, Inc.. It received FDA 510(k) clearance on 1988-08-02 under 510(k) number K882372. The device is classified under product code HQF. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RESUBMITTED DIODE LASER COAGULATOR?

RESUBMITTED DIODE LASER COAGULATOR is a medical device that received FDA 510(k) clearance on 1988-08-02. The listed applicant is CooperVision, Inc.. The 510(k) number is K882372.

When did RESUBMITTED DIODE LASER COAGULATOR receive FDA 510(k) clearance?

RESUBMITTED DIODE LASER COAGULATOR received FDA 510(k) clearance on 1988-08-02, under 510(k) number K882372.

Who is the listed applicant for RESUBMITTED DIODE LASER COAGULATOR?

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

What is the FDA product code for RESUBMITTED DIODE LASER COAGULATOR?

The FDA product code for RESUBMITTED DIODE LASER COAGULATOR is HQF.

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Related Devices (Code: HQF)

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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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