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FDA 510(k)

POREX QUALITY PLASTIC SURGERY INSTRUMENTS

K-Number: K872947 · 1987-08-21

ApplicantPorex Medical
Decision Date1987-08-21
Product CodeKDG
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

POREX QUALITY PLASTIC SURGERY 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 1987-08-21 under 510(k) number K872947. The device is classified under product code KDG. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POREX QUALITY PLASTIC SURGERY INSTRUMENTS?

POREX QUALITY PLASTIC SURGERY INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1987-08-21. The listed applicant is Porex Medical. The 510(k) number is K872947.

When did POREX QUALITY PLASTIC SURGERY INSTRUMENTS receive FDA 510(k) clearance?

POREX QUALITY PLASTIC SURGERY INSTRUMENTS received FDA 510(k) clearance on 1987-08-21, under 510(k) number K872947.

Who is the listed applicant for POREX QUALITY PLASTIC SURGERY 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 QUALITY PLASTIC SURGERY INSTRUMENTS?

The FDA product code for POREX QUALITY PLASTIC SURGERY INSTRUMENTS is KDG.

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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 LOCATORK873044POREX OTOLOGY 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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Related Devices (Code: KDG)

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.

K952678STA-CLEAR ALCOHOL-FREE ENDOSCOPIC ANTI-FOG KITAvail-Southwest DivisionK952200OMNI-JUGWaterstone Medical, Inc.K894785SURGICAL CHISEL/OSTEOTOMEFdt Precision Machine Co., Inc.K891471SIL-MED WASTE FLUID DUMP BAGSil-Med Corp.K872092OSTEOTOME SET, HOKE, STRAIGHT, SET OF 5Military Engineering, Inc.K842824CHERMEL BONE CHISELSCher Mel Corp.

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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