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)

INTERFACE TRANSFUSION BLOOD FILTER #30

K-Number: K823261 · 1983-01-07

ApplicantMedical, Inc.
Decision Date1983-01-07
Product CodeCAK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INTERFACE TRANSFUSION BLOOD FILTER #30 is the device name listed in this FDA 510(k) record. The listed applicant is Medical, Inc.. It received FDA 510(k) clearance on 1983-01-07 under 510(k) number K823261. The device is classified under product code CAK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTERFACE TRANSFUSION BLOOD FILTER #30?

INTERFACE TRANSFUSION BLOOD FILTER #30 is a medical device that received FDA 510(k) clearance on 1983-01-07. The listed applicant is Medical, Inc.. The 510(k) number is K823261.

When did INTERFACE TRANSFUSION BLOOD FILTER #30 receive FDA 510(k) clearance?

INTERFACE TRANSFUSION BLOOD FILTER #30 received FDA 510(k) clearance on 1983-01-07, under 510(k) number K823261.

Who is the listed applicant for INTERFACE TRANSFUSION BLOOD FILTER #30?

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

What is the FDA product code for INTERFACE TRANSFUSION BLOOD FILTER #30?

The FDA product code for INTERFACE TRANSFUSION BLOOD FILTER #30 is CAK.

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 Medical, Inc. 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 21 devices →

Related Devices (Code: CAK)

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.

↑