DISPOSABLE SYRINGE
K-Number: K950969 · 1995-11-29
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Device Summary
Frequently Asked Questions
What is the DISPOSABLE SYRINGE?
DISPOSABLE SYRINGE is a medical device that received FDA 510(k) clearance on 1995-11-29. The listed applicant is Surgiplast , Ltd.. The 510(k) number is K950969.
When did DISPOSABLE SYRINGE receive FDA 510(k) clearance?
DISPOSABLE SYRINGE received FDA 510(k) clearance on 1995-11-29, under 510(k) number K950969.
Who is the listed applicant for DISPOSABLE SYRINGE?
The FDA 510(k) record lists Surgiplast , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DISPOSABLE SYRINGE?
The FDA product code for DISPOSABLE SYRINGE 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 Surgiplast , Ltd. 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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