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FDA 510(k)

WOODLYN CLASSIC TRIAL LENS SET

K-Number: K841766 · 1984-06-01

ApplicantWoodlyn, Inc.
Decision Date1984-06-01
Product CodeHPC
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

WOODLYN CLASSIC TRIAL LENS SET is the device name listed in this FDA 510(k) record. The listed applicant is Woodlyn, Inc.. It received FDA 510(k) clearance on 1984-06-01 under 510(k) number K841766. The device is classified under product code HPC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WOODLYN CLASSIC TRIAL LENS SET?

WOODLYN CLASSIC TRIAL LENS SET is a medical device that received FDA 510(k) clearance on 1984-06-01. The listed applicant is Woodlyn, Inc.. The 510(k) number is K841766.

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

WOODLYN CLASSIC TRIAL LENS SET received FDA 510(k) clearance on 1984-06-01, under 510(k) number K841766.

Who is the listed applicant for WOODLYN CLASSIC TRIAL LENS SET?

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

What is the FDA product code for WOODLYN CLASSIC TRIAL LENS SET?

The FDA product code for WOODLYN CLASSIC TRIAL LENS SET is HPC.

Related Clinical Trials

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.

Other records listing Woodlyn, Inc. as applicant

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.

View all 19 devices →

Related Devices (Code: HPC)

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.

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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