SYRINGES
K-Number: K760392 · 1976-11-02
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Device Summary
Frequently Asked Questions
What is the SYRINGES?
SYRINGES is a medical device that received FDA 510(k) clearance on 1976-11-02. The listed applicant is B. Braun Instruments. The 510(k) number is K760392.
When did SYRINGES receive FDA 510(k) clearance?
SYRINGES received FDA 510(k) clearance on 1976-11-02, under 510(k) number K760392.
Who is the listed applicant for SYRINGES?
The FDA 510(k) record lists B. Braun Instruments as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SYRINGES?
The FDA product code for SYRINGES is FMF.
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 Instruments 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: FMF)
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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