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FDA 510(k)

H200 HANNA SUCTION TREPHINE SYSTEM FOR CORNEAL SUR

K-Number: K896473 · 1990-02-09

ApplicantEmory University School of Medicine
Decision Date1990-02-09
Product CodeHPN
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

H200 HANNA SUCTION TREPHINE SYSTEM FOR CORNEAL SUR is the device name listed in this FDA 510(k) record. The listed applicant is Emory University School of Medicine. It received FDA 510(k) clearance on 1990-02-09 under 510(k) number K896473. The device is classified under product code HPN. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the H200 HANNA SUCTION TREPHINE SYSTEM FOR CORNEAL SUR?

H200 HANNA SUCTION TREPHINE SYSTEM FOR CORNEAL SUR is a medical device that received FDA 510(k) clearance on 1990-02-09. The listed applicant is Emory University School of Medicine. The 510(k) number is K896473.

When did H200 HANNA SUCTION TREPHINE SYSTEM FOR CORNEAL SUR receive FDA 510(k) clearance?

H200 HANNA SUCTION TREPHINE SYSTEM FOR CORNEAL SUR received FDA 510(k) clearance on 1990-02-09, under 510(k) number K896473.

Who is the listed applicant for H200 HANNA SUCTION TREPHINE SYSTEM FOR CORNEAL SUR?

The FDA 510(k) record lists Emory University School of Medicine as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for H200 HANNA SUCTION TREPHINE SYSTEM FOR CORNEAL SUR?

The FDA product code for H200 HANNA SUCTION TREPHINE SYSTEM FOR CORNEAL SUR is HPN.

Related Clinical Trials

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Related Devices (Code: HPN)

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.

K905237EYE SEE INSTRUMENTKing Tool, Inc.K880855PAREL RARE EARTH MAGNET, I.O.M., INTRAOCULAR MAGRichard James, Inc.K860960RARE EARTH INTRA-OCULAR MAGNETAmeritek, Inc.K831702RARE-EARTH INTRA-OCULAR MAGNETMiami Eye Technology, 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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