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FDA 510(k)

TRIAL LENS SET

K-Number: K821082 · 1982-06-14

ApplicantMedical Equipment Designs, Inc.
Decision Date1982-06-14
Product CodeHLH
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

TRIAL LENS SET is the device name listed in this FDA 510(k) record. The listed applicant is Medical Equipment Designs, Inc.. It received FDA 510(k) clearance on 1982-06-14 under 510(k) number K821082. The device is classified under product code HLH. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRIAL LENS SET?

TRIAL LENS SET is a medical device that received FDA 510(k) clearance on 1982-06-14. The listed applicant is Medical Equipment Designs, Inc.. The 510(k) number is K821082.

When did TRIAL LENS SET receive FDA 510(k) clearance?

TRIAL LENS SET received FDA 510(k) clearance on 1982-06-14, under 510(k) number K821082.

Who is the listed applicant for TRIAL LENS SET?

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

What is the FDA product code for TRIAL LENS SET?

The FDA product code for TRIAL LENS SET is HLH.

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Other records listing Medical Equipment Designs, Inc. as applicant

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Related Devices (Code: HLH)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K821083P.D. METERMedical Equipment Designs, Inc.

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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