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FDA 510(k)

MEDPOR OCULAR PEG SYSTEM AND ACCESSORIES

K-Number: K960859 · 1996-05-29

ApplicantPorex Technologies Corp. of Georgia
Decision Date1996-05-29
Product CodeHPZ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MEDPOR OCULAR PEG SYSTEM AND ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Porex Technologies Corp. of Georgia. It received FDA 510(k) clearance on 1996-05-29 under 510(k) number K960859. The device is classified under product code HPZ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDPOR OCULAR PEG SYSTEM AND ACCESSORIES?

MEDPOR OCULAR PEG SYSTEM AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 1996-05-29. The listed applicant is Porex Technologies Corp. of Georgia. The 510(k) number is K960859.

When did MEDPOR OCULAR PEG SYSTEM AND ACCESSORIES receive FDA 510(k) clearance?

MEDPOR OCULAR PEG SYSTEM AND ACCESSORIES received FDA 510(k) clearance on 1996-05-29, under 510(k) number K960859.

Who is the listed applicant for MEDPOR OCULAR PEG SYSTEM AND ACCESSORIES?

The FDA 510(k) record lists Porex Technologies Corp. of Georgia as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDPOR OCULAR PEG SYSTEM AND ACCESSORIES?

The FDA product code for MEDPOR OCULAR PEG SYSTEM AND ACCESSORIES is HPZ.

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Other records listing Porex Technologies Corp. of Georgia 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.

K884884OSSICULAR PROSTHESIS: 8 PARTIAL, 3 TOTAL

Related Devices (Code: HPZ)

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.

K212741EZYPORFci (France Chirurgie Instrumentation) SasK123764DURETTE OCULAR IMPLANTOculo-Plastik, Inc.K110554BIOCERAMIC ORBITAL IMPLANT, ORBTEXCeramisys, Ltd.K112176SILICONE SPHERESOculo Plastik, Inc.K083342ORBITAL RECONSTRUCTIVE IMPLANT IIEvera Medical, Inc.K082850EYE SPHERESProduct and Educational Services, LLC

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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