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FDA 510(k)

NIDEK MODEL AC-2300

K-Number: K932836 · 1993-11-22

ApplicantNidek, Inc.
Decision Date1993-11-22
Product CodeHQF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

NIDEK MODEL AC-2300 is the device name listed in this FDA 510(k) record. The listed applicant is Nidek, Inc.. It received FDA 510(k) clearance on 1993-11-22 under 510(k) number K932836. 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 NIDEK MODEL AC-2300?

NIDEK MODEL AC-2300 is a medical device that received FDA 510(k) clearance on 1993-11-22. The listed applicant is Nidek, Inc.. The 510(k) number is K932836.

When did NIDEK MODEL AC-2300 receive FDA 510(k) clearance?

NIDEK MODEL AC-2300 received FDA 510(k) clearance on 1993-11-22, under 510(k) number K932836.

Who is the listed applicant for NIDEK MODEL AC-2300?

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

What is the FDA product code for NIDEK MODEL AC-2300?

The FDA product code for NIDEK MODEL AC-2300 is HQF.

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Other records listing Nidek, Inc. 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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