TERUMO RETRACTABLE NEEDLE (RN) SYRINGE
K-Number: K953940 · 1996-05-21
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Device Summary
Frequently Asked Questions
What is the TERUMO RETRACTABLE NEEDLE (RN) SYRINGE?
TERUMO RETRACTABLE NEEDLE (RN) SYRINGE is a medical device that received FDA 510(k) clearance on 1996-05-21. The listed applicant is Terumo Medical Corp.. The 510(k) number is K953940.
When did TERUMO RETRACTABLE NEEDLE (RN) SYRINGE receive FDA 510(k) clearance?
TERUMO RETRACTABLE NEEDLE (RN) SYRINGE received FDA 510(k) clearance on 1996-05-21, under 510(k) number K953940.
Who is the listed applicant for TERUMO RETRACTABLE NEEDLE (RN) SYRINGE?
The FDA 510(k) record lists Terumo Medical Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TERUMO RETRACTABLE NEEDLE (RN) SYRINGE?
The FDA product code for TERUMO RETRACTABLE NEEDLE (RN) 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 Terumo Medical Corp. 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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