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FDA 510(k)

PCTE MICROPOROUS MEMBRANE FILTER

K-Number: K870196 · 1987-05-12

ApplicantPoretics Corp.
Decision Date1987-05-12
Product CodeKET
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

PCTE MICROPOROUS MEMBRANE FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Poretics Corp.. It received FDA 510(k) clearance on 1987-05-12 under 510(k) number K870196. The device is classified under product code KET. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PCTE MICROPOROUS MEMBRANE FILTER?

PCTE MICROPOROUS MEMBRANE FILTER is a medical device that received FDA 510(k) clearance on 1987-05-12. The listed applicant is Poretics Corp.. The 510(k) number is K870196.

When did PCTE MICROPOROUS MEMBRANE FILTER receive FDA 510(k) clearance?

PCTE MICROPOROUS MEMBRANE FILTER received FDA 510(k) clearance on 1987-05-12, under 510(k) number K870196.

Who is the listed applicant for PCTE MICROPOROUS MEMBRANE FILTER?

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

What is the FDA product code for PCTE MICROPOROUS MEMBRANE FILTER?

The FDA product code for PCTE MICROPOROUS MEMBRANE FILTER is KET.

Related Clinical Trials

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Related Devices (Code: KET)

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.

K875122DISPOSABLE STERILE SYRINGE FILTERSCorning Medical & ScientificK844671CORNING DISPOSAL STERILE FILTER SYSTEM-NYLONCorning Medical & ScientificK840556DISPOSABLE SYRINGE FILTERSCorning Medical & ScientificK792633STERILIZATION PROCESS/OUTERWRAPProcter & Gamble Mfg. Co.

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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