EXEL SECURETOUCH PTP SYRINGE
K-Number: K011754 · 2003-01-22
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Device Summary
Frequently Asked Questions
What is the EXEL SECURETOUCH PTP SYRINGE?
EXEL SECURETOUCH PTP SYRINGE is a medical device that received FDA 510(k) clearance on 2003-01-22. The listed applicant is Exelint Intl. Co.. The 510(k) number is K011754.
When did EXEL SECURETOUCH PTP SYRINGE receive FDA 510(k) clearance?
EXEL SECURETOUCH PTP SYRINGE received FDA 510(k) clearance on 2003-01-22, under 510(k) number K011754.
Who is the listed applicant for EXEL SECURETOUCH PTP SYRINGE?
The FDA 510(k) record lists Exelint Intl. Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EXEL SECURETOUCH PTP SYRINGE?
The FDA product code for EXEL SECURETOUCH PTP SYRINGE is MEG.
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 Exelint Intl. Co. 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: MEG)
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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