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FDA 510(k)

CORNING DISPOSAL STERILE FILTER SYSTEM-NYLON

K-Number: K844671 · 1985-02-25

Decision Date1985-02-25
Product CodeKET
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

CORNING DISPOSAL STERILE FILTER SYSTEM-NYLON is the device name listed in this FDA 510(k) record. The listed applicant is Corning Medical & Scientific. It received FDA 510(k) clearance on 1985-02-25 under 510(k) number K844671. 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 CORNING DISPOSAL STERILE FILTER SYSTEM-NYLON?

CORNING DISPOSAL STERILE FILTER SYSTEM-NYLON is a medical device that received FDA 510(k) clearance on 1985-02-25. The listed applicant is Corning Medical & Scientific. The 510(k) number is K844671.

When did CORNING DISPOSAL STERILE FILTER SYSTEM-NYLON receive FDA 510(k) clearance?

CORNING DISPOSAL STERILE FILTER SYSTEM-NYLON received FDA 510(k) clearance on 1985-02-25, under 510(k) number K844671.

Who is the listed applicant for CORNING DISPOSAL STERILE FILTER SYSTEM-NYLON?

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

What is the FDA product code for CORNING DISPOSAL STERILE FILTER SYSTEM-NYLON?

The FDA product code for CORNING DISPOSAL STERILE FILTER SYSTEM-NYLON is KET.

Related Clinical Trials

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.

Other records listing Corning Medical & Scientific 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.

View all 111 devices →

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.

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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