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FDA 510(k)

CATARACT TRAY

K-Number: K842647 · 1985-05-09

ApplicantDeroyal Industries, Inc.
Decision Date1985-05-09
Product CodeHNN
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

CATARACT TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Deroyal Industries, Inc.. It received FDA 510(k) clearance on 1985-05-09 under 510(k) number K842647. The device is classified under product code HNN. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CATARACT TRAY?

CATARACT TRAY is a medical device that received FDA 510(k) clearance on 1985-05-09. The listed applicant is Deroyal Industries, Inc.. The 510(k) number is K842647.

When did CATARACT TRAY receive FDA 510(k) clearance?

CATARACT TRAY received FDA 510(k) clearance on 1985-05-09, under 510(k) number K842647.

Who is the listed applicant for CATARACT TRAY?

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

What is the FDA product code for CATARACT TRAY?

The FDA product code for CATARACT TRAY is HNN.

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Related Devices (Code: HNN)

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.

K110166CLEARCUT S SAFETY KNIFEAlcon Research, Ltd.K922378OPHTHALMIC KNIFEMicroptics Development LaboratoryK882402RETRACTIVE INCISION MICROMETER (RIM) GUAGEOptical CenterK881669MVR/STILETTO BLADE 20GA. - P/N 1900Advanced Surgical Products, Inc.K874979PRISMA DISPOSABLE MVR/STILETTO BLADEAdvanced Surgical Products, Inc.K874057OPHTHALMIC TIP & BLADE SCALPELSMyocure, 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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