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)

ULTIPOR SOLUTION CONTAINER FILTER

K-Number: K790879 · 1979-06-01

Decision Date1979-06-01
Product CodeFPB
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ULTIPOR SOLUTION CONTAINER FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Pall Biomedical Products Co.. It received FDA 510(k) clearance on 1979-06-01 under 510(k) number K790879. The device is classified under product code FPB. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTIPOR SOLUTION CONTAINER FILTER?

ULTIPOR SOLUTION CONTAINER FILTER is a medical device that received FDA 510(k) clearance on 1979-06-01. The listed applicant is Pall Biomedical Products Co.. The 510(k) number is K790879.

When did ULTIPOR SOLUTION CONTAINER FILTER receive FDA 510(k) clearance?

ULTIPOR SOLUTION CONTAINER FILTER received FDA 510(k) clearance on 1979-06-01, under 510(k) number K790879.

Who is the listed applicant for ULTIPOR SOLUTION CONTAINER FILTER?

The FDA 510(k) record lists Pall Biomedical Products Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ULTIPOR SOLUTION CONTAINER FILTER?

The FDA product code for ULTIPOR SOLUTION CONTAINER FILTER is FPB.

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 Pall Biomedical Products Co. 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 28 devices →

Related Devices (Code: FPB)

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.

↑