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FDA 510(k)

POREX OTOLOGY INSTRUMENTS

K-Number: K873044 · 1987-09-04

ApplicantPorex Medical
Decision Date1987-09-04
Product CodeLRC
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

POREX OTOLOGY INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Porex Medical. It received FDA 510(k) clearance on 1987-09-04 under 510(k) number K873044. The device is classified under product code LRC. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POREX OTOLOGY INSTRUMENTS?

POREX OTOLOGY INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1987-09-04. The listed applicant is Porex Medical. The 510(k) number is K873044.

When did POREX OTOLOGY INSTRUMENTS receive FDA 510(k) clearance?

POREX OTOLOGY INSTRUMENTS received FDA 510(k) clearance on 1987-09-04, under 510(k) number K873044.

Who is the listed applicant for POREX OTOLOGY INSTRUMENTS?

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

What is the FDA product code for POREX OTOLOGY INSTRUMENTS?

The FDA product code for POREX OTOLOGY INSTRUMENTS is LRC.

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Other records listing Porex Medical 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.

K872791POREX NERVE LOCATORK872947POREX QUALITY PLASTIC SURGERY INSTRUMENTSK863946POREX(TM) EXTRA-OCULAR ORBITAL IMPLANTK863943POREX(TM) EYE SPHERE IMPLANTK870257POREX(TM) SILICONE SURGICAL IMPLANTS FOR E.N.T.K870154POREX(TM) TISSUE EXPANDER

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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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