DEVON STANDARD SYRINGE, HYPODERMIC NEEDLE AND INSULIN SYRINGE
K-Number: K052551 · 2005-09-30
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Device Summary
Frequently Asked Questions
What is the DEVON STANDARD SYRINGE, HYPODERMIC NEEDLE AND INSULIN SYRINGE?
DEVON STANDARD SYRINGE, HYPODERMIC NEEDLE AND INSULIN SYRINGE is a medical device that received FDA 510(k) clearance on 2005-09-30. The listed applicant is Devon Safety Products, Inc.. The 510(k) number is K052551.
When did DEVON STANDARD SYRINGE, HYPODERMIC NEEDLE AND INSULIN SYRINGE receive FDA 510(k) clearance?
DEVON STANDARD SYRINGE, HYPODERMIC NEEDLE AND INSULIN SYRINGE received FDA 510(k) clearance on 2005-09-30, under 510(k) number K052551.
Who is the listed applicant for DEVON STANDARD SYRINGE, HYPODERMIC NEEDLE AND INSULIN SYRINGE?
The FDA 510(k) record lists Devon Safety Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DEVON STANDARD SYRINGE, HYPODERMIC NEEDLE AND INSULIN SYRINGE?
The FDA product code for DEVON STANDARD SYRINGE, HYPODERMIC NEEDLE AND INSULIN 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 Devon Safety Products, Inc. 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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