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)

BUSSE PLASTIC LOR SYRINGE

K-Number: K080804 · 2008-07-09

Decision Date2008-07-09
Product CodeCAZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

BUSSE PLASTIC LOR SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Busse Hosipital Disposables. It received FDA 510(k) clearance on 2008-07-09 under 510(k) number K080804. The device is classified under product code CAZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BUSSE PLASTIC LOR SYRINGE?

BUSSE PLASTIC LOR SYRINGE is a medical device that received FDA 510(k) clearance on 2008-07-09. The listed applicant is Busse Hosipital Disposables. The 510(k) number is K080804.

When did BUSSE PLASTIC LOR SYRINGE receive FDA 510(k) clearance?

BUSSE PLASTIC LOR SYRINGE received FDA 510(k) clearance on 2008-07-09, under 510(k) number K080804.

Who is the listed applicant for BUSSE PLASTIC LOR SYRINGE?

The FDA 510(k) record lists Busse Hosipital Disposables as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BUSSE PLASTIC LOR SYRINGE?

The FDA product code for BUSSE PLASTIC LOR SYRINGE is CAZ.

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 Busse Hosipital Disposables 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.

Related Devices (Code: CAZ)

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.

↑