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FDA 510(k)

DOHLMAN DOANE KERATOPROTHESIS

K-Number: K915062 · 1992-01-21

ApplicantMackeen Consultants, Ltd.
Decision Date1992-01-21
Product CodeHQM
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

DOHLMAN DOANE KERATOPROTHESIS is the device name listed in this FDA 510(k) record. The listed applicant is Mackeen Consultants, Ltd.. It received FDA 510(k) clearance on 1992-01-21 under 510(k) number K915062. The device is classified under product code HQM. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DOHLMAN DOANE KERATOPROTHESIS?

DOHLMAN DOANE KERATOPROTHESIS is a medical device that received FDA 510(k) clearance on 1992-01-21. The listed applicant is Mackeen Consultants, Ltd.. The 510(k) number is K915062.

When did DOHLMAN DOANE KERATOPROTHESIS receive FDA 510(k) clearance?

DOHLMAN DOANE KERATOPROTHESIS received FDA 510(k) clearance on 1992-01-21, under 510(k) number K915062.

Who is the listed applicant for DOHLMAN DOANE KERATOPROTHESIS?

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

What is the FDA product code for DOHLMAN DOANE KERATOPROTHESIS?

The FDA product code for DOHLMAN DOANE KERATOPROTHESIS is HQM.

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.

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Other records listing Mackeen Consultants, Ltd. 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.

K852737LACTOPLATE

Related Devices (Code: HQM)

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.

K182986Boston Keratoprosthesis, Type I LuciaMassachusetts Eye and Ear Infirmary D/B/A BostonK121203BOSTON KERATOPROSTHESIS OR BOSTON KPROMassachusetts Eye & Ear InfirmaryK013756ALPHACOR; ALPHACOR-A (FOR AHAKIC EYES); ALPHACOR-P (FOR PHAKIC OR PSEUDOPHAKIC EYES)Argus Biomedical Pty, Ltd.

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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