Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

DISPOSABLE STERILE FILTER SYSTEM

K-Number: K831450 · 1983-06-02

Decision Date1983-06-02
Product CodeLIB
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE STERILE FILTER SYSTEM 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 1983-06-02 under 510(k) number K831450. The device is classified under product code LIB. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE STERILE FILTER SYSTEM?

DISPOSABLE STERILE FILTER SYSTEM is a medical device that received FDA 510(k) clearance on 1983-06-02. The listed applicant is Corning Medical & Scientific. The 510(k) number is K831450.

When did DISPOSABLE STERILE FILTER SYSTEM receive FDA 510(k) clearance?

DISPOSABLE STERILE FILTER SYSTEM received FDA 510(k) clearance on 1983-06-02, under 510(k) number K831450.

Who is the listed applicant for DISPOSABLE STERILE FILTER SYSTEM?

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 DISPOSABLE STERILE FILTER SYSTEM?

The FDA product code for DISPOSABLE STERILE FILTER SYSTEM is LIB.

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: LIB)

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑