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)

BRAUN HEMOSTASIS INTRODUCERS

K-Number: K955820 · 1996-03-25

Decision Date1996-03-25
Product CodeDYB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BRAUN HEMOSTASIS INTRODUCERS is the device name listed in this FDA 510(k) record. The listed applicant is B.Braun Medical, Inc.. It received FDA 510(k) clearance on 1996-03-25 under 510(k) number K955820. The device is classified under product code DYB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BRAUN HEMOSTASIS INTRODUCERS?

BRAUN HEMOSTASIS INTRODUCERS is a medical device that received FDA 510(k) clearance on 1996-03-25. The listed applicant is B.Braun Medical, Inc.. The 510(k) number is K955820.

When did BRAUN HEMOSTASIS INTRODUCERS receive FDA 510(k) clearance?

BRAUN HEMOSTASIS INTRODUCERS received FDA 510(k) clearance on 1996-03-25, under 510(k) number K955820.

Who is the listed applicant for BRAUN HEMOSTASIS INTRODUCERS?

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

What is the FDA product code for BRAUN HEMOSTASIS INTRODUCERS?

The FDA product code for BRAUN HEMOSTASIS INTRODUCERS is DYB.

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 B.Braun 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 142 devices →

Related Devices (Code: DYB)

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.

↑