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FDA 510(k)

DAELIM CORP. EYE WEAR MODEL

K-Number: K932612 · 1994-04-06

ApplicantDaelim Corp.
Decision Date1994-04-06
Product CodeHQZ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

DAELIM CORP. EYE WEAR MODEL is the device name listed in this FDA 510(k) record. The listed applicant is Daelim Corp.. It received FDA 510(k) clearance on 1994-04-06 under 510(k) number K932612. The device is classified under product code HQZ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DAELIM CORP. EYE WEAR MODEL?

DAELIM CORP. EYE WEAR MODEL is a medical device that received FDA 510(k) clearance on 1994-04-06. The listed applicant is Daelim Corp.. The 510(k) number is K932612.

When did DAELIM CORP. EYE WEAR MODEL receive FDA 510(k) clearance?

DAELIM CORP. EYE WEAR MODEL received FDA 510(k) clearance on 1994-04-06, under 510(k) number K932612.

Who is the listed applicant for DAELIM CORP. EYE WEAR MODEL?

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

What is the FDA product code for DAELIM CORP. EYE WEAR MODEL?

The FDA product code for DAELIM CORP. EYE WEAR MODEL is HQZ.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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