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FDA 510(k)

TOPCON EC-200 ENDO-PHOTOCOAGULATOR LASER

K-Number: K903421 · 1990-12-18

ApplicantTop Con
Decision Date1990-12-18
Product CodeHQF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

TOPCON EC-200 ENDO-PHOTOCOAGULATOR LASER is the device name listed in this FDA 510(k) record. The listed applicant is Top Con. It received FDA 510(k) clearance on 1990-12-18 under 510(k) number K903421. 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 TOPCON EC-200 ENDO-PHOTOCOAGULATOR LASER?

TOPCON EC-200 ENDO-PHOTOCOAGULATOR LASER is a medical device that received FDA 510(k) clearance on 1990-12-18. The listed applicant is Top Con. The 510(k) number is K903421.

When did TOPCON EC-200 ENDO-PHOTOCOAGULATOR LASER receive FDA 510(k) clearance?

TOPCON EC-200 ENDO-PHOTOCOAGULATOR LASER received FDA 510(k) clearance on 1990-12-18, under 510(k) number K903421.

Who is the listed applicant for TOPCON EC-200 ENDO-PHOTOCOAGULATOR LASER?

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

What is the FDA product code for TOPCON EC-200 ENDO-PHOTOCOAGULATOR LASER?

The FDA product code for TOPCON EC-200 ENDO-PHOTOCOAGULATOR LASER is 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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