BUSSE PLASTIC LOR SYRINGE
K-Number: K080804 · 2008-07-09
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Device Summary
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.
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