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)

UNIMIX CONAINER-EMPTY CONTAINER W/3 LEAD TRANS.SET

K-Number: K932477 · 1994-06-10

Decision Date1994-06-10
Product CodeKPE
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

UNIMIX CONAINER-EMPTY CONTAINER W/3 LEAD TRANS.SET is the device name listed in this FDA 510(k) record. The listed applicant is Baxter Healthcare Corp. It received FDA 510(k) clearance on 1994-06-10 under 510(k) number K932477. The device is classified under product code KPE. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UNIMIX CONAINER-EMPTY CONTAINER W/3 LEAD TRANS.SET?

UNIMIX CONAINER-EMPTY CONTAINER W/3 LEAD TRANS.SET is a medical device that received FDA 510(k) clearance on 1994-06-10. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K932477.

When did UNIMIX CONAINER-EMPTY CONTAINER W/3 LEAD TRANS.SET receive FDA 510(k) clearance?

UNIMIX CONAINER-EMPTY CONTAINER W/3 LEAD TRANS.SET received FDA 510(k) clearance on 1994-06-10, under 510(k) number K932477.

Who is the listed applicant for UNIMIX CONAINER-EMPTY CONTAINER W/3 LEAD TRANS.SET?

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

What is the FDA product code for UNIMIX CONAINER-EMPTY CONTAINER W/3 LEAD TRANS.SET?

The FDA product code for UNIMIX CONAINER-EMPTY CONTAINER W/3 LEAD TRANS.SET is KPE.

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 Baxter Healthcare Corp 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 504 devices →

Related Devices (Code: KPE)

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.

↑