RAMY PISTON SYRINGE
K-Number: K971664 · 1997-07-25
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Device Summary
Frequently Asked Questions
What is the RAMY PISTON SYRINGE?
RAMY PISTON SYRINGE is a medical device that received FDA 510(k) clearance on 1997-07-25. The listed applicant is Alshifa Medical Syringes Mfg. Co., Ltd.. The 510(k) number is K971664.
When did RAMY PISTON SYRINGE receive FDA 510(k) clearance?
RAMY PISTON SYRINGE received FDA 510(k) clearance on 1997-07-25, under 510(k) number K971664.
Who is the listed applicant for RAMY PISTON SYRINGE?
The FDA 510(k) record lists Alshifa Medical Syringes Mfg. Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RAMY PISTON SYRINGE?
The FDA product code for RAMY PISTON 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 Alshifa Medical Syringes Mfg. Co., 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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