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FDA 510(k)

GRC-WT, GRC-W

K-Number: K843899 · 1985-01-28

ApplicantOlympus Corp.
Decision Date1985-01-28
Product CodeHKI
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

GRC-WT, GRC-W is the device name listed in this FDA 510(k) record. The listed applicant is Olympus Corp.. It received FDA 510(k) clearance on 1985-01-28 under 510(k) number K843899. The device is classified under product code HKI. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GRC-WT, GRC-W?

GRC-WT, GRC-W is a medical device that received FDA 510(k) clearance on 1985-01-28. The listed applicant is Olympus Corp.. The 510(k) number is K843899.

When did GRC-WT, GRC-W receive FDA 510(k) clearance?

GRC-WT, GRC-W received FDA 510(k) clearance on 1985-01-28, under 510(k) number K843899.

Who is the listed applicant for GRC-WT, GRC-W?

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

What is the FDA product code for GRC-WT, GRC-W?

The FDA product code for GRC-WT, GRC-W is HKI.

Other records listing Olympus 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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